Causes of Seizures - intellectual deficit due to hydroxylysinuria
Causes of Seizures - intellectual deficit due to hydroxylysinuria (Diseases Database):
The follow list shows some of the possible medical causes of Seizures - intellectual deficit due to hydroxylysinuria
that are listed by the Diseases Database:
- Nortriptyline
- Systemic lupus erythematosus
- Peroxisomal acyl-CoA oxidase deficiency
- Diffuse sclerosis of Schilder
- Epilepsy, primary
- Acute intermittent porphyria
- Microphthalmia-dermal aplasia-sclerocornea syndrome
- Alcohol withdrawal syndrome
- Cysticercosis
- Sickle cell crisis (thrombotic)
- Intraspinal abscess / granuloma
- Cycloserine
- Galactosialidosis
- Amphotericin B
- Bicuculline
- Alpha-L-iduronidase deficiency
- Parry-Romberg syndrome
- Aicardi's syndrome
- Cavernous haemangioma
- X-linked periventricular heterotopia
- Neurofibromatosis type 1
- Imipenem
- I-cell disease
- Benign Rolandic epilepsy
- Vertebrobasilar dolichoectasia
- Guanidinoacetate methyltransferase deficiency
- Aluminium (dialysis related) toxicity
- Zunich neuroectodermal syndrome
- Griscelli syndrome type 2
- Arginosuccinate synthetase deficiency
- Ramon syndrome
- Acute disseminated encephalomyelitis
- Arginase deficiency
- Water hemlock poisoning
- Lidocaine
- Methionine malabsorption
- Fructose intolerance
- Bupivacaine
- Ceroid lipofuscinosis neuronal type 8
- Thebaine
- Multiple sclerosis
- Maple syrup urine disease
- Carbon monoxide toxicity
- D-glycerate kinase deficiency
- Fumarase deficiency
- Sotos syndrome
- Malaria
- McLeod neuroacanthocytosis syndrome
- Alpers disease
- Haw River syndrome
- Intraventricular haemorrhage
- Bifunctional peroxisomal enzyme deficiency
- Glycerol kinase deficiency
- GM1 gangliosidosis, type 2
- Toxoplasma, congenital
- Corpus callosum agenesis type 2
- Benign neonatal epilepsy
- Aminomethyltransferase deficiency
- Pyruvate dehydrogenase deficiency
- Malaria (malignant tertian)
- Worster-Drought syndrome
- Renal failure, chronic
- Meningoencephalitis
- Gamma hydroxybutyrate
- Tyrosinaemia type 2
- Mefenamic acid
- Chester porphyria
- Sulphite oxidase deficiency
- Progressive encephalopathy-edema-hypsarrhythmia-optic atrophy syndrome
- Porphobilinogen synthase deficiency
- Recessive deafness-onychodystrophy-osteodystrophy-retardation syndrome
- Gabapentin
- Febrile convulsion
- Neonatal hypoglycaemia
- Glucose transporter type 1 deficiency
- Malignant hypertension
- Takayasu's arteritis
- Glycine decarboxylase deficiency
- Sjogren-Larsson syndrome
- Aminophylline
- Endometriosis
- Hyponatraemia
- Fat embolism
- Generalized gangliosidosis GM1
- Aicardi Goutieres syndrome
- Coproporphyria, hereditary
- Seitelberger's disease
- Seemanova-Lesny syndrome
- Temporal lobe epilepsy
- Methylenetetrahydrofolate reductase deficiency
- Meningioma
- Rett syndrome
- Adenylosuccinate lyase deficiency
- Ceroid lipofuscinosis, neuronal 4
- Birth hypoxia
- Walker-Warburg syndrome
- Nalidixic acid
- Nikethamide
- Alexander disease
- Sturge-Weber syndrome
- Hypocalcaemia
- Ramsay Hunt syndrome
- Schistosoma japonicum
- Ohtahara syndrome
- Tuberous sclerosis
- Malonyl-CoA decarboxylase deficiency
- Kohlschutter syndrome
- Hypomagnesemia
- Cerebral venous sinus thrombosis
- Neurocysticercosis
- Isoniazid
- Chromosome 7q deletion syndrome
- Hallervorden-Spatz disease
- Rubinstein-Taybi syndrome
- Benign familial infantile convulsions
- Congenital muscular dystrophy, autosomal recessive
- Hypophosphataemia
- Subdural haemorrhage
- Norfloxacin
- Cyanides
- Lithium
- Carbohydrate deficient glycoprotein syndrome type 1a
- Dihydropteridine reductase deficiency
- Intracranial space-occupying lesion
- CADASIL
- Tay-Sachs disease
- Eclampsia
- Dentatorubropallidoluysian degeneration
- Crome syndrome
- Rabies
- Sanjad-Sakati syndrome
- Epidural haemorrhage
- Romano-Ward syndrome
- Ornithine carbamyltransferase deficiency
- Glutathione synthase deficiency
- Unverricht-Lundborg syndrome
- Hypoglycaemia
- Sandhoff's disease
- Hartnup's disease
- Borjeson-Forssman-Lehmann syndrome
- Angelman's syndrome
- Bupropion
- Thrombotic thrombocytopenic purpura
- Respiratory failure
- Fukuyama congenital muscular dystrophy
- Asphyxiation
- Chloroquine
- Oculocerebrocutaneous syndrome
- Ceroid lipofuscinosis, neuronal 1, infantile
- Severe myoclonic epilepsy in infancy
- Intracranial arteriovenous malformation
- Cerebrohepatorenal syndrome
- Ciprofloxacin
- Menke disease
- Giant axonal neuropathy
- Absence seizure
- MELAS
- Strychnine
- Salaam attacks
- GM2 gangliosidosis type AB
- Desipramine
- Paraneoplastic limbic encephalitis
- Fryns syndrome 2
- Carbon tetrachloride
- Dyke-Davidoff-Masson syndrome
- Salla disease
- Cocaine
- MERRF
- Mefloquine
- Posterior leucoencephalopathy syndrome
- Succinic semialdehyde dehydrogenase deficiency
- Sphingomyelinase deficiency
- Lead
- Dihydropyrimidine dehydrogenase deficiency
- Phosphoethanolaminuria
- Polyarteritis nodosa
- Rasmussen encephalitis
- Rud's syndrome
- Lafora body disease
- Nasu-Hakola disease
- Sialidosis type 1
- Cystathionine beta-synthase deficiency
- Dothiepin
- Epidermal naevus syndrome
- Landau-Kleffner syndrome
- Athabaskan brain stem dysgenesis
- Ceroid lipofuscinosis, neuronal 3, juvenile
- Amitriptyline
- Schizencephaly
- 6-Pyruvoyl tetrahydropterin synthase deficiency
- Intracranial abscess / granuloma
- Ceroid lipofuscinosis neuronal 2 late infantile
- X-linked mental retardation 1
- Tramadol
- Lennox-Gastaut syndrome
- Muscle-eye-brain disease
- Chromosome 12p tetrasomy syndrome
- van der Knaap disease
- Erythropoietin
- Sarcoidosis
- Cerebellar dyssynergia
Source: Diseases Database
Seizures - intellectual deficit due to hydroxylysinuria Causes: Book Excerpts
- Differential Diagnosis - Seizures/Convulsions
- Differential Diagnosis - Seizures – Childhood
- Differential Diagnosis - Seizures – Neonatal
- Medical causes - Seizures, absence
- Medical causes - Seizures, complex partial
- Medical causes - Seizures, generalized tonic-clonic
- Medical causes - Seizures, simple partial
- Medical causes - Seizures, absence
- Medical causes - Seizures, complex partial
- Medical causes - Seizures, generalized tonic-clonic
- Medical causes - Seizures, simple partial
- Differential Overview
- Seizures
- Medical causes - Seizures, generalized tonic-clonic
- Medical causes - Seizures, complex partial
- Medical causes - Seizures, generalized tonic-clonic
- Medical causes - Seizures, simple partial
- Principal Causes of Seizures - Seizures
- Medical causes - Seizures, absence
- Medical causes - Seizures, complex partial
- Medical causes - Seizures, generalized tonic-clonic
- Medical causes - Seizures, simple partial
Seizures - intellectual deficit due to hydroxylysinuria as a complication of other conditions:
Other conditions that might have
Seizures - intellectual deficit due to hydroxylysinuria as a complication may,
potentially, be an underlying cause of Seizures - intellectual deficit due to hydroxylysinuria.
Our database lists the following as having
Seizures - intellectual deficit due to hydroxylysinuria as a complication of that condition:
Seizures - intellectual deficit due to hydroxylysinuria as a symptom:
Conditions listing Seizures - intellectual deficit due to hydroxylysinuria
as a symptom may also be potential underlying causes of Seizures - intellectual deficit due to hydroxylysinuria.
Our database lists the following as having
Seizures - intellectual deficit due to hydroxylysinuria as a symptom of that condition:
- 1q deletion
- 1q terminal deletion
- 2-Hydroxyglutaricaciduria
- 2-Methylbutyric Aciduria
- 2-methylbutyryl-coenzyme A dehydrogenase deficiency
- 22q11.2 deletion syndrome
- 2q deletion
- 3-Hydroxyisobutyric aciduria
- 3-methylglutaconic aciduria, type 4
- 4-hydroxyphenylacetic aciduria
- Absence of septum pellucidum and septo-optic dysplasia
- Absent corpus callosum - cataract - immunodeficiency
- Acanthamoeba infection
- Acanthamoeba infection of the central nervous system
- Achalasia - addisonianism - alacrima syndrome
- Achalasia - Addisonianism - Alacrimia syndrome
- Achalasia - adrenal - alacrima syndrome
- Acid-Base Imbalance
- Acidemia, methylmalonic
- Ackee Fruit Food poisoning
- Acrocallosal syndrome
- Acrocallosal Syndrome (Schinzel Type)
- Acute Disseminated Encephalomyelitis
- Acute meningitis
- Acyl-CoA dehydrogenase, short chain, deficiency of
- Adams Nance syndrome
- ADANE
- Adducted thumb syndrome recessive form
- Adducted thumbs - arthrogryposis, Christian type
- Adrenoleukodystrophy
- Adrenoleukodystrophy, autosomal, neonatal form
- Adult low grade infiltrative supratentorial Astrocytoma
- African Sleeping sickness
- Agenesis of the corpus callosum
- Agnathia-holoprosencephaly-situs inversus
- Aicardi-Goutieres syndrome 1
- Aicardi-Goutieres syndrome 2
- Aicardi-Goutieres syndrome 3
- Aicardi-Goutieres syndrome 4
- Aicardi-Goutieres syndrome 5
- Akesson syndrome
- Al Gazali - Nair syndrome
- Al Gazali Sabrinathan Nair syndrome
- Albright's hereditary osteodystrophy
- Alcohol Withdrawal
- Alexander Syndrome
- Allergic encephalomyelitis
- Alopecia mental retardation syndrome
- Alopecia, epilepsy, oligophrenia syndrome of Moynahan
- Alopecia, epilepsy, pyorrhea, mental subnormality
- Alpers Syndrome
- Alpha-N-acetylgalactosaminidase deficiency, Type III
- Alternating Hemiplegia
- Aluminium toxicity
- Aminoacylase 1 deficiency
- Amnesic shellfish poisoning
- Amphetamine abuse
- Ampola syndrome
- Amyloid angiopathy
- Amyloidosis VII
- Amyloidosis, familial cutaneous
- Amyloidosis, oculoleptomeningeal
- Aneurysm, intracranial berry
- Aneurysm, intracranial berry, 1
- Aneurysm, intracranial berry, 2
- Aneurysm, intracranial berry, 3
- Aneurysm, intracranial berry, 4
- Aneurysm, intracranial berry, 5
- Aneurysm, intracranial berry, 6
- Aneurysm, intracranial berry, 7
- Aneurysm, intracranial berry, 8
- Aneurysmal subarachnoid haemorrhage
- Angelman syndrome
- Anoxia
- Antepartum Eclampsia
- Apricot seed poisoning
- Arachnoid Cysts
- Arakawa's syndrome 2
- Arbovirosis
- Arginase deficiency
- Argininosuccinic aciduria
- Arizona Bark Scorpion poisoning
- Arnold-Chiari malformation type 4
- Arteriovenous Malformation
- Arthrogryposis - epileptic seizures - migrational brain disorder
- Arthrogryposis, congenital - myopathic seizures
- Aspartylglucosaminidase deficiency
- Aspartylglucosaminuria
- Aspartylglycosaminuria
- Ataxia - apraxia - mental retardation, X-linked
- Ataxia Telangiectasia
- Athabaskan brainstem dysgenesis
- Athabaskan severe combined immunodeficiency
- Atherosclerosis, premature - deafness - diabetes mellitus - photomyoclonus - nephropathy - degenerative neurologic disease
- Atherosclerosis- deafness - diabetes - epilepsy - nephropathy
- Atkin-Flatiz syndrome
- Atlantic mussel food poisoning
- ATR-X syndrome
- Atypical pyridoxine-dependent seizures
- Autoimmune limbic encephalitis
- Autoimmune thyroid disease associated Celiac Disease
- Autoimmune Vasculitis
- Autonomic Dysreflexia
- Azalea poisoning
- Bacterial meningitis
- Baló disease
- Baneberry poisoning
- Bannayan-Zonana syndrome
- Baraitser Brett Piesowicz syndrome
- Baraitser-Rodeck-Garner syndrome
- Barbiturate abuse
- Batten Disease
- Benign familial neonatal-infantile seizures
- Benzodiazepine abuse
- Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification
- Beta ketothiolase deficiency
- Beta-hydroxybutyric aciduria
- Binswanger's Disease
- Biotinidase deficiency, late onset
- Bird cherry seed poisoning
- Bitter almond seed poisoning
- Bone marrow failure - neurologic abnormalities
- Borjeson Syndrome
- Boudhina-Yedes-Khiari syndrome
- Brain - bone - fat
- Brain cancer
- Brain tumor, adult
- Branchio-skeleto-genital syndrome
- Brown snake poisoning
- Brugada Syndrome
- Bufotenine poisoning
- Busulfan toxicity syndrome
- Calcification of basal ganglia with or without hypocalcemia
- California encephalitis
- Canavan leukodystrophy
- Carbamoyl-phosphate synthase 1 deficiency
- Carnitine palmitoyl transferase 1 deficiency
- Carnitine palmitoyl transferase 2 deficiency
- Carnitine palmitoyl transferase deficiency
- Carnitine palmitoyl transferase II deficiency, infantile hepatocardiomuscular type
- Carnitine palmitoyl transferase II deficiency, lethal neonatal form
- Carnitine-acylcarnitine translocase deficiency
- Catastrophic Antiphospholipid Syndrome
- Caterpillar complication poisoning
- Celiac Disease
- Celiac disease - epilepsy - occipital calcifications
- Celiac disease, susceptibility to 1
- Celiac disease, susceptibility to 10
- Celiac disease, susceptibility to 11
- Celiac disease, susceptibility to 12
- Celiac disease, susceptibility to 13
- Celiac disease, susceptibility to 2
- Celiac disease, susceptibility to 3
- Celiac disease, susceptibility to 4
- Celiac disease, susceptibility to 5
- Celiac disease, susceptibility to 6
- Celiac disease, susceptibility to 7
- Celiac disease, susceptibility to 8
- Celiac disease, susceptibility to 9
- Cerebellar abscess
- Cerebellar atrophy with progressive microcephaly
- Cerebellar hypoplasia
- Cerebral abscess
- Cerebral astrocytoma, adult
- Cerebral calcification cerebellar hypoplasia
- Cerebral hemorrhage
- Cerebral Palsy
- Cerebral palsy, spastic, diplegic
- Cerebral sarcoma
- Cerebral ventricle neoplasm
- Cerebro oculo skeleto renal syndrome
- Cerebrorenodigital syndrome
- Ceroid lipofuscinosis, neuronal
- Ceroid lipofuscinosis, neuronal 1, infantile
- Ceroid lipofuscinosis, neuronal 5
- Ceroid lipofuscinosis, neuronal 6, late infantile
- Ceroid lipofuscinosis, neuronal 7
- Ceroid lipofuscinosis, neuronal 8
- Ceroid lipofuscinosis, neuronal 9
- Chediak-Higashi like syndrome
- Chemical poisoning - 1,1-Dimethylhydrazine
- Chemical poisoning - 1-Propanol
- Chemical poisoning - 2-Methyl-4-Chlorophenoxyacetic Acid
- Chemical poisoning - 4-Aminopyridine
- Chemical poisoning - Acetone
- Chemical poisoning - Acetonitrile
- Chemical poisoning - Acrylamide
- Chemical poisoning - Acrylonitrile
- Chemical poisoning - Adiponitrile
- Chemical poisoning - Alanycarb
- Chemical poisoning - Aldicarb
- Chemical poisoning - Aldoxycarb
- Chemical poisoning - Allyxycarb
- Chemical poisoning - Aluminum
- Chemical poisoning - Amidithion
- Chemical poisoning - Aminocarb
- Chemical poisoning - Amiton
- Chemical poisoning - Amitraz
- Chemical poisoning - Ammonium Bifluoride
- Chemical poisoning - Ammonium Nitrate
- Chemical poisoning - Ammonium Sulfamate
- Chemical poisoning - Aniline
- Chemical poisoning - Arsine
- Chemical poisoning - Athyl-Gusathion
- Chemical poisoning - Azinfos-methyl
- Chemical poisoning - Azinfosethyl
- Chemical poisoning - Azinophos-methyl
- Chemical poisoning - Azinphos
- Chemical poisoning - Azinphos-ethyl
- Chemical poisoning - Azinphos-methyl
- Chemical poisoning - Azinphosmetile
- Chemical poisoning - Azothoate
- Chemical poisoning - Bendiocarb
- Chemical poisoning - Benfuracarb
- Chemical poisoning - Benoxafos
- Chemical poisoning - Benzene
- Chemical poisoning - Borates
- Chemical poisoning - Boric Acid
- Chemical poisoning - Bromates
- Chemical poisoning - Bromethalin
- Chemical poisoning - Bromophos
- Chemical poisoning - Bromophos-ethyl
- Chemical poisoning - Bufencarb
- Chemical poisoning - Butacarb
- Chemical poisoning - Butocarboxim
- Chemical poisoning - Butoxcarboxim
- Chemical poisoning - Cadmium
- Chemical poisoning - Cadusafos
- Chemical poisoning - Carbanolate
- Chemical poisoning - Carbaryl
- Chemical poisoning - Carbinoxamine
- Chemical poisoning - Carbofuran
- Chemical poisoning - Carbon Disulfide
- Chemical poisoning - Carbon Tetrachloride
- Chemical poisoning - Carbophenothion
- Chemical poisoning - Carbosulfan
- Chemical poisoning - Chlorate salts
- Chemical poisoning - Chlorfenvinphos
- Chemical poisoning - Chloromethane
- Chemical poisoning - Chloropyrifos
- Chemical poisoning - Chlorpyrifos
- Chemical poisoning - Chlorpyrifos methyl
- Chemical poisoning - Cloethocarb
- Chemical poisoning - Coumaphos
- Chemical poisoning - Cresols
- Chemical poisoning - Cresylic acid
- Chemical poisoning - Cyanthoate
- Chemical poisoning - Decarbofuran
- Chemical poisoning - Demeton
- Chemical poisoning - Demeton-methyl
- Chemical poisoning - Demeton-O
- Chemical poisoning - Demeton-O-methyl
- Chemical poisoning - Demeton-S-methyl
- Chemical poisoning - Demeton-S-methylsulphon
- Chemical poisoning - Dialifos
- Chemical poisoning - Diazinon
- Chemical poisoning - Dichlorvos
- Chemical poisoning - Dicresyl
- Chemical poisoning - Dicrotophos
- Chemical poisoning - Dimetan
- Chemical poisoning - Dimethoate
- Chemical poisoning - Dimethylnitrosamine
- Chemical poisoning - Dimetilan
- Chemical poisoning - Dinitrophenol
- Chemical poisoning - Dioxacarb
- Chemical poisoning - Dioxathion
- Chemical poisoning - Disulfiram
- Chemical poisoning - Disulfoton
- Chemical poisoning - EMPC
- Chemical poisoning - Endothion
- Chemical poisoning - Ethiofencarb
- Chemical poisoning - Ethion
- Chemical poisoning - Ethoate-methyl
- Chemical poisoning - Ethoprophos
- Chemical poisoning - Ethyl-guthion
- Chemical poisoning - Ethylene Glycol
- Chemical poisoning - Ethylene Oxide
- Chemical poisoning - Etrimfos
- Chemical poisoning - Fenchlorphos
- Chemical poisoning - Fenethacarb
- Chemical poisoning - Fenitrothion
- Chemical poisoning - Fenobucarb
- Chemical poisoning - Fensulfothion
- Chemical poisoning - Fenthion
- Chemical poisoning - Fonophos
- Chemical poisoning - Formothion
- Chemical poisoning - Furathiocarb
- Chemical poisoning - Glufosinate
- Chemical poisoning - Guthion (ethyl)
- Chemical poisoning - Helium
- Chemical poisoning - Heptenophos
- Chemical poisoning - High Melting Explosive (HMX)
- Chemical poisoning - Hydrogen Sulfide
- Chemical poisoning - Hyquincarb
- Chemical poisoning - Incense
- Chemical poisoning - Iodofenphos
- Chemical poisoning - Isoprocarb
- Chemical poisoning - Lysergic Acid Diethylamide
- Chemical poisoning - Malathion
- Chemical poisoning - Mecarbam
- Chemical poisoning - Metaldehyde
- Chemical poisoning - Methacrifos
- Chemical poisoning - Methamidophos
- Chemical poisoning - Methidathion
- Chemical poisoning - Methiocarb
- Chemical poisoning - Methomyl
- Chemical poisoning - Metiltriazotion
- Chemical poisoning - Metolcarb
- Chemical poisoning - Mevinphos
- Chemical poisoning - Mexacarbate
- Chemical poisoning - Monocrotophos
- Chemical poisoning - Monosodium Methanarsenate
- Chemical poisoning - Mouth Wash
- Chemical poisoning - Nitrilacarb
- Chemical poisoning - Nitrites
- Chemical poisoning - Omethoate
- Chemical poisoning - Oxamyl
- Chemical poisoning - Oxydeprofos
- Chemical poisoning - Oxydisulfoton
- Chemical poisoning - Parathion
- Chemical poisoning - Parathion Methyl
- Chemical poisoning - Phencyclidine
- Chemical poisoning - Phenkapton
- Chemical poisoning - Phorate
- Chemical poisoning - Phosalone
- Chemical poisoning - Phosdrin
- Chemical poisoning - Phosmet
- Chemical poisoning - Phosphamidon
- Chemical poisoning - Phosphine
- Chemical poisoning - Phoxim
- Chemical poisoning - Pirimicarb
- Chemical poisoning - Pirimiphos-methyl
- Chemical poisoning - Primiphos methyl
- Chemical poisoning - Profenofos
- Chemical poisoning - Promacyl
- Chemical poisoning - Promecarb
- Chemical poisoning - Propane
- Chemical poisoning - Propoxur
- Chemical poisoning - Propylene Glycol
- Chemical poisoning - Prothidathion
- Chemical poisoning - Prothoate
- Chemical poisoning - Pyrethrin
- Chemical poisoning - Pyrimitate
- Chemical poisoning - Quinalphos
- Chemical poisoning - Quintiofos
- Chemical poisoning - Selenious Acid
- Chemical poisoning - Sodium Monofluoroacetate
- Chemical poisoning - Sophamide
- Chemical poisoning - Strychnine
- Chemical poisoning - Sulfotep
- Chemical poisoning - Tazimcarb
- Chemical poisoning - Terbufos
- Chemical poisoning - Tetraethyl Pyrophosphate
- Chemical poisoning - Tetramethylammonium Hydroxide
- Chemical poisoning - Tetramethylenedisulfotetramine
- Chemical poisoning - Thallium Sulfate
- Chemical poisoning - Thiocarboxime
- Chemical poisoning - Thiodicarb
- Chemical poisoning - Thiofanox
- Chemical poisoning - Thiometon
- Chemical poisoning - Tolclofos methyl
- Chemical poisoning - Toxaphene
- Chemical poisoning - Triazophos
- Chemical poisoning - Triazotion
- Chemical poisoning - Trichloroethylene
- Chemical poisoning - Trifenfos
- Chemical poisoning - Trimethacarb
- Chemical poisoning - Tungsten
- Chemical poisoning - Turpentine Oil
- Chemical poisoning - Vamidothion
- Chemical poisoning - Vinyl Choride
- Chemical poisoning - White Phosphorus
- Chemical poisoning - XMC
- Chemical poisoning - Xylylcarb
- Cherry laurel seed poisoning
- Cherry seed poisoning
- Childhood-onset cerebral X-linked adrenoleukodystrophy
- Chokecherry seed poisoning
- Choreoacanthocytosis amyotrophic
- Choroid Plexus neoplasms
- Choroido cerebral calcification syndrome infantile form
- Christmas Rose poisoning
- Chromosome 1, 1p36 deletion syndrome
- Chromosome 1, monosomy 1q4
- Chromosome 1, pter-p36
- Chromosome 1, Terminal deletion
- Chromosome 1, uniparental disomy 1q12 q21
- Chromosome 11q duplication syndrome
- Chromosome 12, 12p trisomy
- Chromosome 12, Isochromosome 12p Mosaic
- Chromosome 12p deletion
- Chromosome 12p deletion syndrome
- Chromosome 12p duplication syndrome
- Chromosome 12p tetrasomy syndrome
- Chromosome 14 Ring
- Chromosome 14q deletion syndrome
- Chromosome 14q, partial deletion
- Chromosome 15 inverted duplication
- Chromosome 15q, partial duplication (distal q arm)
- Chromosome 15q, partial duplication (unbalanced translocation)
- Chromosome 15q13.3 microdeletion syndrome
- Chromosome 17 ring
- Chromosome 17 trisomy mosaicism
- Chromosome 17, deletion 17q23 q24
- Chromosome 17p, partial deletion
- Chromosome 18 deletion syndrome
- Chromosome 18 Ring
- Chromosome 18q, partial deletion
- Chromosome 19p duplication syndrome
- Chromosome 1p deletion syndrome
- Chromosome 1p duplication syndrome
- Chromosome 1q deletion
- Chromosome 2, monosomy 2pter p24
- Chromosome 2, monosomy 2q
- Chromosome 2, monosomy 2q24
- Chromosome 2, monosomy 2q37
- Chromosome 20, deletion 20p
- Chromosome 20p deletion syndrome
- Chromosome 21 monosomy
- Chromosome 22 Ring
- Chromosome 22, trisomy
- Chromosome 22q deletion
- Chromosome 22q11.2 deletion syndrome
- Chromosome 22q13 deletion
- Chromosome 22q13.3 deletion syndrome
- Chromosome 3, trisomy 3p
- Chromosome 3, trisomy 3q
- Chromosome 4 ring syndrome
- Chromosome 4 short arm deletion
- Chromosome 4, Monosomy 4q
- Chromosome 4, trisomy 4p
- Chromosome 4p deletion syndrome
- Chromosome 5, Trisomy 5p
- Chromosome 5, trisomy 5pter p13 3
- Chromosome 5, trisomy 5q
- Chromosome 5p duplication syndrome
- Chromosome 5q duplication syndrome
- Chromosome 6, monosomy 6q
- Chromosome 6, trisomy 6q
- Chromosome 6q deletion syndrome
- Chromosome 6q duplication syndrome
- Chromosome 7, monosomy 7q3
- Chromosome 7, trisomy 7q
- Chromosome 7q duplication syndrome
- Chromosome 8 recombinant syndrome
- Chromosome 8, trisomy 8q
- Chromosome 8q duplication syndrome
- Chromosome 9, monosomy 9p
- Chromosome 9, trisomy 9p
- Chromosome 9p deletion syndrome
- Chromosome diploid-triploid mosaicism syndrome
- Citrullinemia
- Citrullinemia I
- Citrullinemia II
- Classic childhood ALD
- Classical pyridoxine-dependent seizures
- Claviceps purpurea poisoning
- Cobra poisoning
- Cocaine abuse
- Cocaine overdose
- Cockayne syndrome
- Codeine overdose
- Coenzyme Q 10 (CoQ10), deficiency
- Coffin-Lowry syndrome
- Coleman Randall syndrome
- Collagenous celiac disease
- Colpocephaly
- Complex 1 mitochondrial respiratory chain deficiency
- Complex 2 mitochondrial respiratory chain deficiency
- Complex 5 mitochondrial respiratory chain deficiency
- Congenital cystic eye, multiple ocular and intracranial anomalies
- Congenital cytomegalovirus
- Congenital disorder of glycosylation type 1/IIX
- Congenital disorder of glycosylation type 1D
- Congenital disorder of glycosylation type 1E
- Congenital disorder of glycosylation type 1F
- Congenital disorder of glycosylation type 1G
- Congenital disorder of glycosylation type 1I
- Congenital disorder of glycosylation type 1J
- Congenital disorder of glycosylation type 1K
- Congenital disorder of glycosylation type 1L
- Congenital disorder of glycosylation type 1M
- Congenital disorder of glycosylation type 1X
- Congenital disorder of glycosylation type 2A
- Congenital disorder of glycosylation type 2B
- Congenital disorder of glycosylation type 2C
- Congenital disorder of glycosylation type IIH
- Congenital disorder of glycosylation, type In
- Congenital Disorders of Glycosylation
- Congenital hepatic porphyria
- Congenital herpes simplex
- Congenital hypoparathyroidism, seizures, growth and mental retardation and unusual facies
- Conversion Disorder
- Copper deficiency, familial benign
- Corpus callosum agenesis-neuropathy
- Corpus callosum dysgenesis X-linked recessive
- Cortes-Lacassie syndrome
- Craniosynostosis
- Craniosynostosis Fontaine type
- Craniosynostosis mental retardation clefting syndrome
- Craniotelencephalic dysplasia
- Creatine deficiency, X-linked
- Cree leukoencephalopathy
- Creutzfeldt-Jakob Disease
- Crisponi syndrome
- Cutis verticis gyrata mental deficiency
- Cycad poisoning
- Cysticercosis
- Cytochrome c oxydase deficiency, French-Canadian type
- Dandy-Walker - facial hemangioma
- Dandy-Walker malformation with mental retardation, basal ganglia disease, and seizures
- Dandy-Walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy
- De Grouchy Syndrome
- De Sanctis-Cacchione syndrome
- Deadly nightshade (Solanum dulcamara) poisoning
- Deafness - skeletal dysplasia - lip granuloma
- Defect in synthesis of adenosylcobalamin
- Del (1) (pter-p36.3) mosaicism
- Del(1) (pter-p36.2)
- Del(1) (q42-qter)
- Deletion 10q
- Deletion 18q
- Deletion 20p
- Deletion 22q13
- Deletion 2q
- Deletion 2q24
- Deletion 4p
- Deletion 6q
- Delleman-Oorthuys syndrome
- Delphinium poisoning
- Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency
- DEND syndrome
- Dennis cohen syndrome
- Dentatorubral Pallidoluysian Atrophy
- Dermochondrocorneal dystrophy of François
- Desmoplastic cerebral astrocytoma of infancy
- Desmoplastic infantile ganglioma
- Developmental delay - hypotonia extremities hypertrophy
- Developmental delay due to 2-methylbutyryl-CoA dehydrogenase deficiency
- Devriendt syndrome
- Diabetes insipidus, diabetes mellitus, optic atrophy
- Diabetes insipidus, diabetes mellitus, optic atrophy, deafness, mitochondrial form
- Diabetes insipidus, nephrogenic type 2
- Diabetes insipidus, nephrogenic, dominant type
- Diabetes insipidus, nephrogenic, recessive type
- Diabetes Insipidus, Neurogenic
- Diabetic hypoglycemia
- Dialysis encephalopathy syndrome
- DIDMOAD Syndrome, Mitochondrial form
- DiGeorge syndrome
- Digitorenocerebral syndrome
- Dihydropyrimidine dehydrogenase deficiency
- Dionisi-Vici-Sabetta-Gambarara syndrome
- Distinctive Craniofacial Features - Pterygia - Mental Retardation
- Dobriner syndrome
- Down's syndrome associated Celiac Disease
- Dup (1) (q32-qter) and del (7)(q32-qter)
- Dup(1) (q24-q41)
- Duplication 12p
- Duplication 13
- Duplication 5p
- Duplication 5q
- Duplication 6q
- Duplication 7q
- Duplication 8q
- Dysbarism
- Dysequilibrium syndrome
- Dysharmonic skeletal maturation - muscular fiber disproportion
- East African Trypanosomiasis
- Eclampsia
- Ecstasy overdose
- Edinburgh malformation syndrome
- Ehlers-Danlos syndrome with periventricular heterotopia
- Electrocution
- Emanuel syndrome
- Encephalitis
- Encephalo cranio cutaneous lipomatosis
- Encephalocele anterior
- Encephalocele frontal
- Encephaloceles
- Encephalomyelitis
- Encephalopathy due to sulphite oxidase deficiency
- Encephalopathy progressive - optic atrophy
- End-stage renal disease
- Endomyocardial fibroelastosis
- Ependymoma
- Epidermoid carcinoma
- Epilepsy - microcephaly - skeletal dysplasia
- Epilepsy - telangiectasia
- Epilepsy benign neonatal dominant form
- Epilepsy benign neonatal recessive form
- Epilepsy with myoclonic-astatic crisis
- Epilepsy, partial, familial
- Epilepsy, pyridoxin-dependent
- Epilepsy, Pyridoxine-Dependent
- Epilepsy, X-linked - learning disabilities - behavior disorders
- Epileptic encephalopathy, early infantile, 2
- Epileptic encephalopathy, early infantile, 4
- Epiphyseal dysplasia - hearing loss - dysmorphism
- Epiphyseal dysplasia dysmorphism camptodactyly
- Episodic ataxia, type 5
- Episodic ataxia, type 6
- Ethylmalonic aciduria
- Eugenol oil poisoning
- Facial asymetry - temporal seizures
- Facial asymmetry - temporal seizures
- FACWA syndrome
- Fahr's Syndrome
- Familial band heterotopia
- Familial partial epilepsy with variable focus
- Familial porencephaly
- Febrile Seizures
- Feigenbaum-Bergeron-Richardson syndrome
- Fetal warfarin syndrome
- Fetal-onset olivopontocerebellar hypoplasia
- FG Syndrome
- FG syndrome 1
- FG syndrome 2
- FG syndrome 3
- FG syndrome 4
- FG syndrome 5
- Fire Ant bite
- Focal cortical dysplasia type II
- Focal cortical dysplasia type IIA
- Focal cortical dysplasia type IIB
- Folinic acid-responsive seizures
- Foramina parietalia permagna
- Franek-Bocker-Kahlen syndrome
- Fructose intolerance
- Fructose-1,6-bisphosphatase deficiency, hereditary
- Fryns macrocephaly
- Fucosidosis type 1
- Fucosidosis type II
- Fumaric aciduria
- Functioning pancreatic endocrine tumor
- Galloway syndrome
- Ganglioglioma
- Garret-Tripp syndrome
- Gaucher Disease
- Gaucher disease - perinatal lethal form
- Gaucher disease type 2
- Generalized lipodystrophy with mental retardation, deafness, short stature and slender bones
- Genetic reflex epilepsy
- Genée-Wiedemann syndrome
- Giant axonal neuropathy
- Glioma
- Gliomatosis cerebri
- Gliosarcoma
- Glucocorticoid deficiency, familial
- Glutathione synthetase deficiency, severe
- Glycine encephalopathy, atypical mild form
- Glycine encephalopathy, classical neonatal early-onset form
- Glycine encephalopathy, classical neonatal form
- Glycogen storage disease type 1C
- Glycogen storage disease type 1D
- Glycogen Storage Disease Type I
- Glycosylphosphatidylinositol deficiency
- GM2-gangliosidosis, AB variant
- Goldberg syndrome
- Golden Chain tree poisoning
- Grand-Kaine-Fulling syndrome
- Granulomatous amebic encephalitis
- Granulomatous Angiitis of the Central Nervous System
- Griscelli disease
- Griscelli syndrome type II
- Grix-Blankenship-Peterson syndrome
- Guanidinoacetate methyltransferase deficiency
- Gustavson syndrome
- Haas-Robinson syndrome
- Hall-Riggs mental retardation syndrome
- Hallervorden-Spatz disease
- HARD syndrome
- HARD syndrome (Hydrocephalus - agyria - retinal dysplasia)
- Haspeslagh Fryns Muelenaere syndrome
- Heatstroke
- Hemimegalencephaly
- Hemiplegic migraine, familial type 2
- Hemolytic uremic syndrome
- Hemorrhagic shock and encephalopathy syndrome
- Hendra Virus
- Herbal Agent adverse reaction - Ginkgo biloba
- Herbal Agent adverse reaction - Licorice
- Herbal Agent adverse reaction - Margosa oil
- Herbal Agent adverse reaction - Pennyroyal Oil
- Herbal Agent overdose - Golden Seal
- Herbal Agent overdose - Lobelia
- Herbal Agent overdose - Rhubarb
- Hereditary nodular heterotopia
- Heroin overdose
- Herpes, Neonatal
- Herpes, Neonatal - Central Nervous System Infection
- Herpes, Neonatal - Disseminated
- HHV-6 encephalitis
- High altitude cerebral edema
- Hirschsprung disease ganglioneuroblastoma
- HIV/AIDS
- Hoigné syndrome
- Holoprosencephaly
- Homocystinuria
- Homocystinuria syndrome
- Howard-Young syndrome
- Human HOXA1 Syndromes
- Hydranencephaly
- Hydrocarbon poisoning
- Hydrocephalus autosomal recessive
- Hydrocodone overdose
- Hypercoagulability syndrome, due to glycosylphosphatidylinositol deficiency
- Hyperglycinemia
- Hyperinsulinemic hypoglycemia, familial, 4
- Hyperinsulinemic hypoglycemia, familial, 5
- Hyperinsulinemic hypoglycemia, familial, 6
- Hypernatremia
- Hyperprolinemia type 2
- Hypoglycemia
- Hypoglycemia with deficiency of glycogen synthetase in the liver
- Hypoglycemic attack
- Hypomagnesemia 4, renal
- Hypomagnesemia caused by selective magnesium malabsorption
- Hypomagnesemia primary
- Hypomelanosis of Ito
- Hypoparathyroidism - short stature - mental retardation
- Hypoparathyroidism familial isolated
- Hypophosphatasia
- Hypoplastic Left Heart Syndrome
- Hypothalamic hamartomas
- IBIDS syndrome
- Ichthyosis and male hypogonadism
- Ichthyosis male hypogonadism
- Immunosuppressive Measles Encephalitis
- Inborn amino acid metabolism disorder
- Inborn urea cycle disorder
- Incontinentia Pigmenti
- Indian Tobacco poisoning
- Infantile epileptic-dyskinetic encephalopathy
- Infantile sialic acid storage disorder
- Infantile Spasms
- Infantile spasms - broad thumbs
- Insulinoma
- Intestinal pseudoobstruction chronic idiopathic
- Intracranial arachnoid cysts
- Intracranial arteriovenous malformation
- Intrapartum Eclampsia
- Jervell and Lange-Nielsen Syndrome
- Jimsonweed poisoning
- Joubert Syndrome
- Juvenile pilocytic astrocytoma
- Kalam-Hafeez syndrome
- KBG Syndrome
- Kernicterus
- Kidney stones
- Kifafa seizure disorder
- L1 Syndrome
- Lactic Acidosis, Fatal Infantile
- Landau-Kleffner Syndrome
- Leigh syndrome
- Leigh syndrome, French Canadian type
- Leigh syndrome, Saguenay-Lac-St. Jean type
- Lennox-Gastaut Syndrome
- Leucinosis
- Leukemia
- Leukemia, T-Cell
- Leukodystrophy
- Leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema
- Leukomalacia
- Levine-Critchley syndrome
- Limbic encephalitis
- Lindstrom syndrome
- Lissauer paralysis
- Lissencephaly
- Lissencephaly 3
- Lissencephaly type 1, due to LIS 1 anomalies
- Lissencephaly with cerebellar hypoplasia
- Lissencephaly, type 1, X-linked
- Lobelia poisoning
- Lubs X-linked mental retardation syndrome
- Lupus
- Lymphangiectasies and lymphedema Hennekam type
- Lymphoedema - lymphangiectasia - mental retardation
- Lymphomatoid Granulomatosis
- Lysteria monocytoigeneses meningitis
- Macrogyria, pseudobulbar palsy and mental retardation
- Magnesium deficiency
- Malformations in neuronal migration
- Malignant astrocytoma
- Malignant rhabdoid tumors
- Malonic aciduria
- Maple syrup urine disease
- Maple syrup urine disease, type 1A
- Maple syrup urine disease, type 1B
- Maple syrup urine disease, type II
- Maple syrup urine disease, type III
- Mastocytosis - short stature - hearing loss
- Mastocytosis, cutaneous, with short stature, conductive hearing loss and microtia
- Maternally Inherited Leigh Syndrome
- Measles Encephalitis in Children with Immunosuppression
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Megalencephalic leukoencephalopathy with subcortical cysts
- Megalencephaly
- Megalencephaly - polymicrogyria - post-axial polydactyly - hydrocephalus
- Meinecke syndrome
- Melanoma - astrocytoma syndrome
- MELAS
- Melioidosis
- Meninges cancer
- Meningioma
- Meningitis
- Meningococcal disease
- Meningoencephalocele
- Menkes Disease
- Mental retardation - epilepsy, X-linked
- Mental retardation - hypocupremia - hypobetalipoproteinemia
- Mental Retardation - Pterygia - Shortness - Distinctive Facial Appearance
- Mental retardation - short broad thumbs
- Mental retardation progressive spasticity
- Mental retardation progressive spasticity, X-linked
- Mental retardation unusual facies ampola type
- Mental retardation X-linked dysmorphism
- Mental retardation, Smith-Fineman-Myers type
- Mental retardation, Wolff type
- Mental retardation, X-linked - corpus callosum agenesis - spastic quadriparesis
- Mental retardation, X-linked - epilepsy - progressive joint contractures - typical face
- Mental retardation, X-linked - hypotonia - recurrent Infections
- Mental retardation, X-linked - seizures - psoriasis
- Mental retardation, X-linked syndromic 12
- Mental retardation, X-linked with brachydactyly and macroglossia
- Mental retardation, X-linked, 12
- Mental retardation, X-linked, 94
- Mental retardation, X-linked, Armfield type
- Mercury poisoning
- Mercury poisoning - consumption of contaminated fish
- Mercury poisoning - Folk Remedies
- Metabolic disorders
- Metachromatic Leukodystrophy
- Metastatic insulinoma
- Methylene tetrahydrofolate reductase deficiency
- Methylmalonic acidemia, synthesis defect of AdoCbl and MeCbl
- Methylmalonic acidemia, vitamin B12 responsive
- Methylmalonic aciduria - homocystinuria
- Methylmalonic aciduria - microcephaly - cataract
- Methylmalonicaciduria with homocystinuria, cobalamin F
- MGA 4
- Micrencephaly corpus callosum agenesis
- Microcephalic osteodysplastic primordial dwarfism types 1 and 3
- Microcephaly - seizures - mental retardation - heart disorders
- Microcephaly - sparse hair - mental retardation - seizures
- Microcephaly brain defect spasticity hypernatremia
- Microcephaly micropenis convulsions
- Microcephaly, corpus callosum dysgenesis and cleft lip-palate
- Microcephaly, hiatal hernia and nephrotic syndrome
- Microcephaly, mental retardation and tracheoesophageal fistula associated with features of Rett Syndrome
- Microlissencephaly - micromelia
- Microphthalmia - brain atrophy
- Microphthalmia - mental deficiency
- Microphthalmia and mental deficiency
- Microphthalmia syndromic, type 10
- Microphthalmia syndromic, type 5
- Microphthalmia, syndromic 7
- Mild citrullinemia
- Miller-Dieker syndrome
- Mistletoe poisoning
- Mitochondrial diseases
- Mitochondrial diseases, clinically indefinite
- Mitochondrial encephalomyopathy - aminoacidopathy
- Mitochondrial myopathy - lactic acidosis
- MN1
- Monosomy 1p36
- Monosomy 20p
- Moyamoya Disease
- MoyaMoya disease 1
- MoyaMoya disease 2
- MoyaMoya disease 3
- Moyamoya Syndrome
- Mucolipidosis type 1
- Muller-Barth-Menger syndrome
- Multiple carboxylase deficiency, propionic acidemia
- Muscle phosphoglycerate kinase deficiency
- Muscular dystrophy - white matter spongiosis
- Mustard tree poisoning
- Myoclonus hereditary - progressive distal muscular atrophy
- Myoclonus progressive epilepsy of Unverricht and Lundborg
- Myoclonus, cerebellar ataxia, deafness
- Myopathy - growth and mental retardation - hypospadias
- Myopathy - growth delay - mental retardation - hypospadias
- N syndrome
- N-acetyl glutamate synthetase deficiency
- N-acetyl-alpha-D-galactosaminidase
- NADH CoQ reductase, deficiency of
- Naegleria
- Neonatal ALD
- Neonatal bacterial meningitis
- Nephrosis neuronal dysmigration Syndrome
- Neuroaxonal dystrophy, infantile
- Neurocysticercosis
- Neurodegenerative syndrome, X-linked, Bertini type
- Neuroectodermal tumor, primitive
- Neuroectodermal tumors primitive
- Neurofaciodigitorenal syndrome
- Neuronal intranuclear hyaline inclusion disease
- Neuronal intranuclear inclusion disease
- Neuronal Migration Disorders
- Neuropathy - ataxia - retinitis pigmentosa
- Neuropathy ataxia and retinis pigmentosa
- Neurosarcoidosis
- Neurosyphilis
- Neurosyphilis - general paresis
- Neurosyphilis - meningovascular
- Nevus sebaceous of Jadassohn
- Nicolaides-Baraitser syndrome
- Niemann-Pick disease, type C1
- Niemann-Pick disease, type C2
- Nocardiosis
- Non-ketotic hyperglycinemia
- Non-lissencephalic cortical dysplasia
- Norman-Roberts lissencephaly syndrome
- Oculocerebral hypopigmentation syndrome, type Preus
- Oculodentoosseous dysplasia dominant
- Ohtahara Syndrome
- Oligodendroglioma
- Opium overdose
- Organic acidemia
- Oriental Hornet poisoning
- Ornithine transcarbamylase (OTC) Deficiency
- Ornithine Transcarbamylase Deficiency
- Orofaciodigital syndrome type1
- Osteopetrosis lethal
- Oxycontin overdose
- Pachygyria
- Pachygyria - mental retardation - seizures
- Pachygyria, frontotemporal
- Paine syndrome
- Pallister Killian Mosaic Syndrome
- Pallister Mosaic Syndrome Tetrasomy 12p
- Paragonimiases - lung infection
- Paraneoplastic limbic encephalitis
- Parry Romberg Syndrome
- Partial agenesis of corpus callosum
- Partial lissencephaly
- Partington X-linked mental retardation syndrome
- Patterson pseudoleprechaunism syndrome
- Peach seed poisoning
- PEHO-like syndrome
- Penfield syndrome
- Perinatal hypophosphatasia
- Perinatal-lethal Gaucher disease
- Periventricular laminar heterotopia
- Peroxisomal bifunctional enzyme deficiency
- Peroxisomal defects
- Peroxisome biogenesis disorders
- PHACE association
- Phacomatosis pigmentokeratotica
- Phenylketonuria
- PIBIDS syndrome
- Pitt-Hopkins syndrome
- Plant poisoning - Amygdalin
- Plant poisoning - Anthraquinone
- Plant poisoning - Conline
- Plant poisoning - Cyanogenic glycoside
- Plant poisoning - Cytisine
- Plant poisoning - Euphorbiaceae
- Plant poisoning - Hydroquinone
- Plant poisoning - Indole alkaloids
- Plant poisoning - Lobeline
- Plant poisoning - Quinolizidine alkaloids
- Pneumococcal meningitis
- Poisoning
- Polyarteritis nodosa
- Polycystic kidneys, severe infantile, with tuberous sclerosis
- Pontocerebellar Hypoplasia Type 6
- Pontocerebellar hypoplasia type V
- Porencephaly
- Porphyria
- Porphyria, hereditary coproporphyria
- Post-traumatic epilepsy
- Postpartum Eclampsia
- Primary amebic meningoencephalitis
- Primary angiitis of the central nervous system
- Progressive Multifocal Leukoencephalopathy
- Progressive Rubella Panencephalitis
- Proud-Levine-Carpenter syndrome
- Pseudo-torch syndrome
- Pseudoadrenoleukodystrophy
- Pseudoprogeria syndrome
- Psychiatric disorders associated Celiac Disease
- Pterygia - Mental retardation - Distinctive Craniofacial Features
- Pulmonary embolism
- Pyridoxamine 5-prime-phosphate oxidase deficiency
- Pyruvate carboxylase deficiency, Group A
- Pyruvate carboxylase deficiency, Group B
- Pyruvate dehydrogenase phosphatase deficiency
- Quinidine toxicity
- Rabies
- Radiation induced meningioma
- Ramban-Hasharon syndrome
- Ramon Syndrome
- Ramsay Hunt Syndrome Type 2
- Rasmussen encephalitis
- Rathburn disease
- Refractory Celiac Disease
- Respiratory acidosis
- Respiratory alkalosis
- Rett's syndrome
- Rett-like syndrome
- Reye's Syndrome
- Rhabdoid tumor
- Richieri Costa Guion Almeida Cohen syndrome
- Rift Valley Fever
- Rocky Mountain spotted fever
- Rubella panencephalitis
- Sandhaus Ben-Ami syndrome
- Sandhoff Disease
- SBCAD deficiency
- Schilder's Disease
- Schindler disease
- Schindler disease, type 1
- Schindler disease, type 3
- Schinzel Giedion Syndrome
- Schistosomiasis
- Schizencephaly
- Seckel syndrome 3
- Seemanova-Lesny syndrome
- Seizures - intellectual deficit due to hydroxylysinuria
- Seizures mental retardation hair dysplasia
- Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
- Septo-Optic Dysplasia
- Serine deficiency
- Serotoninergic syndrome
- Severe achondroplasia with developmental delay and acanthosis nigricans
- Shaken Baby Syndrome
- Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD)
- Short stature - craniofacial anomalies - genital hypoplasia
- Short stature - microcephaly - seizures - deafness
- Short-Chain Acyl-CoA Dehydrogenase Deficiency
- SIADH
- Sialidosis type 2
- Sialidosis type I
- Sialidosis type II
- Sialuria, Finnish type
- Simian B virus infection
- Sjögren syndrome, secondary
- Skeletal dysplasia - mental retardation
- Sketetal dysplasia coarse facies mental retardation
- Smith-Fineman-Myers syndrome 2
- Soto's Syndrome
- Sphingolipidosis
- Spinocerebellar ataxia 10
- Spinocerebellar degenerescence, book type
- Spondyloepimetaphyseal dysplasia, X linked with mental deterioration
- Spondylometaphyseal dysplasia, Sedaghatian type
- SSADH deficiency (succinic semialdehyde dehydrogenase deficiency)
- St. Anthony's fire
- Stachybotrys chartarum
- Stevenson-Carey syndrome
- Streptococcal Group B invasive disease
- Striatonigral degeneration infantile
- Sturge-Weber Syndrome
- Subacute sclerosing leukoencephalitis
- Subacute Sclerosing Panencephalitis
- Subdural hematoma
- Subependymal nodular heterotopia
- Substance Withdrawal Syndrome
- Sulfite oxidase deficiency
- Susceptibility to Celiac Disease 1
- Susceptibility to Celiac Disease 10
- Susceptibility to Celiac Disease 11
- Susceptibility to Celiac Disease 12
- Susceptibility to Celiac Disease 13
- Susceptibility to Celiac Disease 2
- Susceptibility to Celiac Disease 3
- Susceptibility to Celiac Disease 4
- Susceptibility to Celiac Disease 5
- Susceptibility to Celiac Disease 6
- Susceptibility to Celiac Disease 7
- Susceptibility to Celiac Disease 8
- Susceptibility to Celiac Disease 9
- Syphilis
- Syphilitic aseptic meningitis
- T-cell acute lymphoblastic leukemia
- TAU syndrome
- Taurodontism and disproportionate short stature
- Tay Sachs Disease
- Tay-Sachs disease - juvenile onset
- Telencephalic leukoencephalopathy
- Tetanus
- Tetrahydrobiopterin deficiencies
- Thalamic degeneration symmetrical infantile
- Thiolase deficiency
- Thompson-Baraitser syndrome
- Thoracic dysplasia - hydrocephalus syndrome
- Thrombotic thrombocytopenic purpura, acquired
- Thrombotic thrombocytopenic purpura, congenital
- Thyrocerebral-retinal syndrome
- Togaviridae disease
- Toxic mushrooms - Anticholinergic
- Toxic mushrooms - cyclopeptides
- Toxic mushrooms - Monomethylhydrazine
- Toxic mushrooms - Psychedelic
- Tranebjaerg-Svejgaard syndrome
- Tranquilizer withdrawal
- Transthyretin amyloidosis
- Traumatic Brain Injury
- Tsao-Ellingson syndrome
- Tuberculous meningitis
- Tuberous sclerosis
- Tuberous sclerosis, type 1
- Tuberous sclerosis, type 2
- Turner syndrome associated Celiac Disease
- Type 1 diabetes related Celiac Disease
- Tyrosinemia, type III
- Ultram overdose
- Unusual facies, renal and Mullerian hypoplasia and severe somatic and mental retardation
- Upton Young syndrome
- Urea Cycle Disorders
- Vagneur Triolle Ripert syndrome
- Van Bogaert disease
- Van Bogaert's disease
- Van Bogaert-Scherer-Epstein Disease
- Vanishing white matter leukodystrophy
- Varicella virus antenatal infection
- Vascular malformations of the brain
- Vasculitis hypersensitivity
- Vein of Galen aneurysm
- Velocardiofacial syndrome
- Venlafaxine toxicity
- Ventricular tachycardia, catecholaminergic polymorphic, 1
- Ventricular tachycardia, catecholaminergic polymorphic, 2
- Viral Hemorrhagic Fevers
- Viral meningitis
- Vitiligo mental retardation facial dysmorphism uremia
- Von Gierke Disease
- W syndrome
- Walker-Warburg Syndrome
- Warfarin syndrome
- Warman Mulliken Hayward syndrome
- Waterhouse-Friderichsen syndrome
- Weaver Williams syndrome
- Wegener's granulomatosis
- West African Trypanosomiasis
- West nile encephalitis
- West Nile fever
- Western equine encephalitis
- Western/Eastern/California encephalitis
- Westphal disease
- Wiedemann Grosse Dibbern syndrome
- Wild cherry seed poisoning
- William's syndrome associated Celiac Disease
- Wolcott-Rallison syndrome
- Wolf-Hirschorn syndrome
- Wolfram Syndrome 2
- Wolfram Syndrome, Mitochondrial form
- X chromosome, duplication Xq13 1 q21 1
- X chromosome, trisomy 26-28
- X chromosome, trisomy Xp3
- X chromosome, trisomy Xpter Xq13
- X chromosome, trisomy Xq
- X chromosome, trisomy Xq25
- X-linked alpha thalassemia mental retardation syndrome (ATR-X)
- Xanthomatosis cerebrotendinous
- Young McKeever Squier syndrome
- Zellweger Syndrome
- Zunich neuroectodermal syndrome
- Zunich-Kaye syndrome
Medical news summaries relating to Seizures - intellectual deficit due to hydroxylysinuria:
The following medical news items are relevant to causes of Seizures - intellectual deficit due to hydroxylysinuria:
Related information on causes of Seizures - intellectual deficit due to hydroxylysinuria:
As with all medical conditions,
there may be many causal factors.
Further relevant information on causes of Seizures - intellectual deficit due to hydroxylysinuria may be found in:
Causes of Seizures - intellectual deficit due to hydroxylysinuria: Online Medical Books
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for more information about the causes of Seizures - intellectual deficit due to hydroxylysinuria.
Seizures/Convulsions:
Differential Diagnosis
(In a Page: Signs and Symptoms)
-
Partial seizure (involve only part of the brain)
–Simple (no altered consciousness)
–Complex (with altered consciousness)
-
Generalized seizure (involve both hemispheres)
–Tonic-clonic
–Atonic
–Tonic
–Myoclonic
–Absence
-
Epilepsy
–Recurrent unprovoked seizures of any or multiple types, which may be idiopathic or symptomatic
- Secondary seizure
–Metabolic abnormalities (e.g., electrolyte disturbances, hypoglycemia)
–Drug effects, intoxication, or withdrawal
–Head injury/trauma
–Febrile seizures in children
–Structural lesions (e.g., tumor, subdural hematoma)
–Cerebrovascular etiologies (e.g., cerebral infarct, intracerebral hemorrhage, subarachnoid hemorrhage
–Hypoxic-ischemic encephalopathy
–Infection (e.g., meningitis, encephalitis)
–Hypoxia
- Nonepileptic seizure
–Not associated with abnormal electrical activity in the brain
–Patients with loss of consciousness secondary to cerebral hypoperfusion (fainting, syncope) may occasionally exhibit brief periods of twitching or convulsive movements resembling seizure activity
–Psychological disturbances (pseudoseizure)
-
Inborn errors of metabolism
–Disorders of amino acid metabolism
–Organic acidemias
–Urea cycle disorders
–Mitochondrial disorders
–Peroxisomal disorders
–Glycogen storage disorders
–Disorders of sugar metabolism
-
Rasmussen's encephalitis
–Causes seizures and progressive
hemispheric dysfunction in infants
» READ BOOK EXCERPT ONLINE »
Source: In a Page: Signs and Symptoms, 2004
Seizures – Childhood:
Differential Diagnosis
(In A Page: Pediatric Signs and Symptoms)
-
Febrile seizure
-
Cerebral dysgenesis: Disorders of neuronal migration, heterotopias, lissencephaly
-
Epilepsy syndromes
–Childhood absence
–Juvenile absence
–Juvenile myoclonic epilepsy (JME)
–Benign rolandic epilepsy (BRE)
-
Meningitis/encephalitis (e.g., HSV)
-
Cerebral abscess
-
Postinfectious (e.g., ADEM)
-
Hyponatremia
-
Hypernatremia
-
Hypocalcemia
-
Hypoglycemia
-
Toxins: Ingestions or sedative withdrawal
-
Trauma
-
Pyridoxine deficiency
-
Neoplasm
-
Degenerative
–Alpers disease
–Rett syndrome
–Unterricht-Lundborg disease
–Lafora disease
–Neuronal ceroid lipofuscinosis
-
Genetic
–Angelman syndrome
–Aicardi syndrome
-
Metabolic
–Medium chain acyl-CoA dehydrogenase deficiency (MCAD)
–Myoclonus epilepsy and ragged-red fibers syndrome (MERRF)
–Sialidosis
–Glucose transporter deficiency
–Urea cycle defects
-
Vascular: Stroke, hemorrhage, vasculitis
-
Hashimoto encephalitis
-
Seizure mimics
–Breath-holding spells
–Syncope, convulsive syncope
–Gastroesophageal reflux
–Cardiac arrhythmia
–Movement disorder
–Migraine
–Benign paroxysmal vertigo
–Parasomnia
–Pseudo-seizure
–Rage attack
» READ BOOK EXCERPT ONLINE »
Source: In A Page: Pediatric Signs and Symptoms, 2007
Seizures – Neonatal:
Differential Diagnosis
(In A Page: Pediatric Signs and Symptoms)
-
Hypoxic ishemic encephalopathy
-
Bacterial meningitis/sepsis
-
Stroke
-
Cerebral dysgenesis
-
Electrolyte disturbances
–Hypoglycemia
–Hyponatremia
–Hypomagnesemia
–Hypocalcemia
-
Maternal drug use
–Drug withdrawal after delivery
–Direct effect of drugs, such as cocaine
-
Congenital infections (TORCH)
–Toxoplasmosis
–Syphilis
–Rubella
–CMV
–HSV - HSV encephalitis
-
Intracranial hemorrhage
–Subdural hemorrhage
–Intraparenchymal hemorrhage
–Intraventricular hemorrhage in the premature infant
–Subarachnoid hemorrhage
-
Urea cycle disturbances
-
Smith-Lemli-Opitz syndrome
-
Nonketotic hyperglycinemia
-
Pyridoxine deficiency
-
Fructose dysmetabolism
-
Amino acidurias
–Maple syrup urine disease
–Proprionic acidemia
-
Molybdenum cofactor deficiency
-
Mitochondrial encephalopathy
-
Glucose transporter deficiency
-
Benign etiologies
–Benign idiopathic neonatal seizures (fifth day fits)
–Benign familial neonatal seizures
-
Movements commonly mistaken for seizures
–Benign neonatal sleep myoclonus
–Jitteriness (may be secondary to
hypoglycemia, drug withdrawal, or
idiopathic)
–Gastroesophageal reflux (arching, writhing)
–Breath-holding spell
» READ BOOK EXCERPT ONLINE »
Source: In A Page: Pediatric Signs and Symptoms, 2007
Seizures, absence:
Medical causes
(Handbook of Signs & Symptoms (Third Edition))
Idiopathic epilepsy
Some forms of absence seizure are accompanied by learning disabilities.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Signs & Symptoms (Third Edition), 2006
Seizures, complex partial:
Medical causes
(Handbook of Signs & Symptoms (Third Edition))
Brain abscess
If the brain abscess is in the temporal lobe, complex partial seizures commonly occur after the abscess disappears. Related problems may include a headache, nausea, vomiting, generalized seizures, and a decreased level of consciousness (LOC). The patient may also develop central facial weakness, auditory receptive aphasia, hemiparesis, and ocular disturbances.
Head trauma
Severe trauma to the temporal lobe (especially from a penetrating injury) can produce complex partial seizures months or years later. The seizures may decrease in frequency and eventually stop. Head trauma also causes generalized seizures and behavior and personality changes.
Herpes simplex encephalitis
The herpes simplex virus commonly attacks the temporal lobe, resulting in complex partial seizures. Other features include a fever, a headache, coma, and generalized seizures.
Temporal lobe tumor
Complex partial seizures may be the first sign of a temporal lobe tumor. Other signs and symptoms include a headache, pupillary changes, and mental dullness. Increased intracranial pressure may cause a decreased LOC, vomiting and, possibly, papilledema.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Signs & Symptoms (Third Edition), 2006
Seizures, generalized tonic-clonic:
Medical causes
(Handbook of Signs & Symptoms (Third Edition))
Brain abscess
Generalized seizures may occur in the acute stage of abscess formation or after the abscess disappears. Depending on the size and location of the abscess, a decreased level of consciousness (LOC) varies from drowsiness to deep stupor. Early signs and symptoms reflect increased intracranial pressure (ICP) and include a constant headache, nausea, vomiting, and focal seizures. Typical later features include ocular disturbances, such as nystagmus, impaired vision, and unequal pupils. Other findings vary with the abscess, site but may include aphasia, hemiparesis, abnormal behavior, and personality changes.
Brain tumor
Generalized seizures may occur, depending on the tumor’s location and type. Other findings include a slowly decreasing LOC, a morning headache, dizziness, confusion, focal seizures, vision loss, motor and sensory disturbances, aphasia, and ataxia. Later findings include papilledema, vomiting, increased systolic blood pressure, widening pulse pressure and, eventually, a decorticate posture.
Chronic renal failure
End-stage renal failure produces the rapid onset of twitching, trembling, myoclonic jerks, and generalized seizures. Related signs and symptoms include anuria or oliguria, fatigue, malaise, irritability, decreased mental acuity, muscle cramps, peripheral neuropathies, anorexia, and constipation or diarrhea. Integumentary effects include skin color changes (yellow, brown, or bronze), pruritus, and uremic frost. Other effects include an ammonia breath odor, nausea and vomiting, ecchymoses, petechiae, GI bleeding, mouth and gum ulcers, hypertension, and Kussmaul’s respirations.
Eclampsia
Generalized seizures are a hallmark of eclampsia. Related findings include a severe frontal headache, nausea and vomiting, vision disturbances, increased blood pressure, a fever of up to 104° (40° C), peripheral edema, and sudden weight gain. The patient may also exhibit oliguria, irritability, hyperactive deep tendon reflexes (DTRs), and a decreased LOC.
Encephalitis
Seizures are an early sign of encephalitis, indicating a poor prognosis; they may also occur after recovery as a result of residual damage. Other findings include a fever, a headache, photophobia, nuchal rigidity, neck pain, vomiting, aphasia, ataxia, hemiparesis, nystagmus, irritability, cranial nerve palsies (causing facial weakness, ptosis, dysphagia), and myoclonic jerks.
Epilepsy (idiopathic)
In most cases, the cause of recurrent seizures is unknown.
Head trauma
In severe cases, generalized seizures may occur at the time of injury. (Months later, focal seizures may occur.) Severe head trauma may also cause a decreased LOC, leading to coma; soft-tissue injury of the face, head, or neck; clear or bloody drainage from the mouth, nose, or ears; facial edema; bony deformity of the face, head, or neck; Battle’s sign; and a lack of response to oculocephalic and oculovestibular stimulation. Motor and sensory deficits may occur along with altered respirations. Examination may reveal signs of increasing ICP, such as a decreased response to painful stimuli, nonreactive pupils, bradycardia, increased systolic pressure, and widening pulse pressure. If the patient is conscious, he may exhibit visual deficits, behavioral changes, and a headache.
Hepatic encephalopathy
Generalized seizures may occur late in hepatic encephalopathy. Associated late-stage findings in the comatose patient include fetor hepaticus, asterixis, hyperactive DTRs, and a positive Babinski’s sign.
Hypoglycemia
Generalized seizures usually occur with severe hypoglycemia, accompanied by blurred or double vision, motor weakness, hemiplegia, trembling, excessive diaphoresis, tachycardia, myoclonic twitching, and a decreased LOC.
Hyponatremia
Seizures develop when serum sodium levels fall below 125 mEq/L, especially if the decrease is rapid. Hyponatremia also causes orthostatic hypotension, a headache, muscle twitching and weakness, fatigue, oliguria or anuria, cold and clammy skin, decreased skin turgor, irritability, lethargy, confusion, and stupor or coma. Excessive thirst, tachycardia, nausea, vomiting, and abdominal cramps may also occur. Severe hyponatremia may cause cyanosis and vasomotor collapse, with a thready pulse.
Hypoparathyroidism
Worsening tetany causes generalized seizures. Chronic hypoparathyroidism produces neuromuscular irritability and hyperactive DTRs.
Hypoxic encephalopathy
Besides generalized seizures, hypoxic encephalopathy may produce myoclonic jerks and coma. Later, if the patient has recovered, dementia, visual agnosia, choreoathetosis, and ataxia may occur.
Neurofibromatosis
Multiple brain lesions from neurofibromatosis cause focal and generalized seizures. Inspection reveals café-au-lait spots, multiple skin tumors, scoliosis, and kyphoscoliosis. Related findings include dizziness, ataxia, monocular blindness, and nystagmus.
Stroke
Seizures (focal more commonly than generalized) may occur within 6 months of an ischemic stroke. Associated signs and symptoms vary with the location and extent of brain damage. They include a decreased LOC, contralateral hemiplegia, dysarthria, dysphagia, ataxia, unilateral sensory loss, apraxia, agnosia, and aphasia. The patient may also develop visual deficits, memory loss, poor judgment, personality changes, emotional lability, urine retention or urinary incontinence, constipation, a headache, and vomiting.
Other causes
Arsenic poisoning
Besides generalized seizures, arsenic poisoning may cause a garlicky breath odor, increased salivation, and generalized pruritus. GI effects include diarrhea, nausea, vomiting, and severe abdominal pain. Related effects include diffuse hyperpigmentation; sharply defined edema of the eyelids, face, and ankles; paresthesia of the extremities; alopecia; irritated mucous membranes; weakness; muscle aches; and peripheral neuropathy.
Barbiturate withdrawal
In chronically intoxicated patients, barbiturate withdrawal may produce generalized seizures 2 to 4 days after the last dose. Status epilepticus is possible.
Diagnostic tests
Contrast agents used in radiologic tests may cause generalized seizures.
Drugs
Toxic blood levels of some drugs, such as theophylline, lidocaine, meperidine, penicillins, and cimetidine, may cause generalized seizures. Phenothiazines, tricyclic antidepressants, amphetamines, isoniazid, and vincristine may cause seizures in patients with preexisting epilepsy.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Signs & Symptoms (Third Edition), 2006
Seizures, simple partial:
Medical causes
(Handbook of Signs & Symptoms (Third Edition))
Brain abscess
Seizures can occur in the acute stage of abscess formation or after resolution of the abscess. A decreased LOC varies from drowsiness to deep stupor. Early signs and symptoms reflect increased intracranial pressure and include a constant, intractable headache; nausea; and vomiting. Later signs and symptoms include ocular disturbances, such as nystagmus, decreased visual acuity, and unequal pupils. Other findings vary according to the abscess site and may include aphasia, hemiparesis, and personality changes.
Brain tumor
Focal seizures are commonly the earliest indicators of a brain tumor. The patient may report a morning headache, dizziness, confusion, vision loss, and motor and sensory disturbances. He may also develop aphasia, generalized seizures, ataxia, a decreased LOC, papilledema, vomiting, increased systolic blood pressure, and widening pulse pressure. Eventually, he may assume a decorticate posture.
Head trauma
Any head injury can cause seizures, but penetrating wounds are characteristically associated with focal seizures. The seizures usually begin 3 to 15 months after injury, decrease in frequency after several years, and eventually stop. The patient may develop generalized seizures and a decreased LOC that may progress to coma.
Stroke
A major cause of seizures in patients older than age 50, a stroke may induce focal seizures up to 6 months after its onset. Related effects depend on the type and extent of the stroke, but may include a decreased LOC, contralateral hemiplegia, dysarthria, dysphagia, ataxia, unilateral sensory loss, apraxia, agnosia, and aphasia. A stroke may also cause visual deficits, memory loss, poor judgment, personality changes, emotional lability, a headache, urinary incontinence or retention, and vomiting. It may result in generalized seizures.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Signs & Symptoms (Third Edition), 2006
Seizures, absence:
Medical causes
(Professional Guide to Signs & Symptoms (Fifth Edition))
Idiopathic epilepsy
Some forms of absence seizure are accompanied by learning disabilities.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006
Seizures, complex partial:
Medical causes
(Professional Guide to Signs & Symptoms (Fifth Edition))
Brain abscess
If the brain abscess is in the temporal lobe, complex partial seizures commonly occur after the abscess disappears. Related problems may include headache, nausea, vomiting, generalized seizures, and a decreased level of consciousness (LOC). The patient may also develop central facial weakness, auditory receptive aphasia, hemiparesis, and ocular disturbances.
Head trauma
Severe trauma to the temporal lobe (especially from a penetrating injury) can produce complex partial seizures months or years later. The seizures may decrease in frequency and eventually stop. Head trauma also causes generalized seizures and behavior and personality changes.
Herpes simplex encephalitis
The herpes simplex virus commonly attacks the temporal lobe, resulting in complex partial seizures. Other features include fever, headache, coma, and generalized seizures.
Temporal lobe tumor
Complex partial seizures may be the first sign of this disorder. Other signs and symptoms include headache, pupillary changes, and mental dullness. Increased intracranial pressure may cause a decreased LOC, vomiting and, possibly, papilledema.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006
Seizures, generalized tonic-clonic:
Medical causes
(Professional Guide to Signs & Symptoms (Fifth Edition))
Alcohol withdrawal syndrome
i> Sudden withdrawal from alcohol dependence may cause seizures 7 to 48 hours later as well as status epilepticus. The patient may also be restless and exhibit hallucinations, profuse diaphoresis, and tachycardia.
Brain abscess
Generalized seizures may occur in the acute stage of abscess formation or after the abscess disappears. Depending on the size and location of the abscess, decreased level of consciousness (LOC) varies from drowsiness to deep stupor. Early signs and symptoms reflect increased intracranial pressure (ICP) and include constant headache, nausea, vomiting, and focal seizures. Typical later features include ocular disturbances, such as nystagmus, impaired vision, and unequal pupils. Other findings vary with the abscess site but may include aphasia, hemiparesis, abnormal behavior, and personality changes.
Brain tumor
Generalized seizures may occur, depending on the tumor’s location and type. Other findings include a slowly decreasing LOC, morning headache, dizziness, confusion, focal seizures, vision loss, motor and sensory disturbances, aphasia, and ataxia. Later findings include papilledema, vomiting, increased systolic blood pressure, widening pulse pressure, and (eventually) decorticate posture.
Cerebral aneurysm
Occasionally, generalized seizures may occur with an aneurysmal rupture. Premonitory signs and symptoms may last several days, but onset is typically abrupt with severe headache, nausea, vomiting, and decreased LOC. Depending on the site and amount of bleeding, related signs and symptoms vary but may include nuchal rigidity, irritability, hemiparesis, hemisensory defects, dysphagia, photophobia, diplopia, ptosis, and unilateral pupil dilation.
Chronic renal failure
End-stage renal failure produces rapid onset of twitching, trembling, myoclonic jerks, and generalized seizures. Related signs and symptoms include anuria or oliguria, fatigue, malaise, irritability, decreased mental acuity, muscle cramps, peripheral neuropathies, anorexia, and constipation or diarrhea. Integumentary effects include skin color changes (yellow, brown, or bronze), pruritus, and uremic frost. Other effects include ammonia breath odor, nausea and vomiting, ecchymoses, petechiae, GI bleeding, mouth and gum ulcers, hypertension, and Kussmaul’s respirations.
Eclampsia
Generalized seizures are a hallmark of this disorder. Related findings include severe frontal headache, nausea and vomiting, vision disturbances, increased blood pressure, fever of up to 104° F (40° C), peripheral edema, and sudden weight gain. The patient may also exhibit oliguria, irritability, hyperactive deep tendon reflexes (DTRs), and decreased LOC.
Encephalitis
Seizures are an early sign of this disorder, indicating a poor prognosis; they may also occur after recovery as a result of residual damage. Other findings include fever, headache, photophobia, nuchal rigidity, neck pain, vomiting, aphasia, ataxia, hemiparesis, nystagmus, irritability, cranial nerve palsies (causing facial weakness, ptosis, dysphagia), and myoclonic jerks.
Epilepsy (idiopathic)
In most cases, the cause of recurrent seizures is unknown.
Head trauma
In severe cases, generalized seizures may occur at the time of injury. (Months later, focal seizures may occur.) Severe head trauma may also cause a decreased LOC, leading to coma; soft-tissue injury of the face, head, or neck; clear or bloody drainage from the mouth, nose, or ears; facial edema; bony deformity of the face, head, or neck; Battle’s sign; and lack of response to oculocephalic and oculovestibular stimulation. Motor and sensory deficits may occur along with altered respirations. Examination may reveal signs of increasing ICP, such as decreased response to painful stimuli, nonreactive pupils, bradycardia, increased systolic pressure, and widening pulse pressure. If the patient is conscious, he may exhibit visual deficits, behavioral changes, and headache.
Hepatic encephalopathy
Generalized seizures may occur late in this disorder. Associated late-stage findings in the comatose patient include fetor hepaticus, asterixis, hyperactive DTRs, and a positive Babinski’s sign.
Hypertensive encephalopathy
This life-threatening disorder may cause seizures along with severely increased blood pressure, decreased LOC, intense headache, vomiting, transient blindness, paralysis, and (eventually) Cheyne-Stokes respirations.
Hypoglycemia
Generalized seizures usually occur with severe hypoglycemia, accompanied by blurred or double vision, motor weakness, hemiplegia, trembling, excessive diaphoresis, tachycardia, myoclonic twitching, and decreased LOC.
Hyponatremia
Seizures develop
when serum sodium levels fall below 125 mEq/L, especially if the decrease is rapid. Hyponatremia also causes orthostatic hypotension, headache, muscle twitching and weakness, fatigue, oliguria or anuria, cold and clammy skin, decreased skin turgor, irritability, lethargy, confusion, and stupor or coma. Excessive thirst, tachycardia, nausea, vomiting, and abdominal cramps may also occur. Severe hyponatremia may cause cyanosis and vasomotor collapse, with a thready pulse.
Hypoparathyroidism
Worsening tetany causes generalized seizures. Chronic hypoparathyroidism produces neuromuscular irritability and hyperactive DTRs.
Hypoxic encephalopathy
Besides generalized seizures, this disorder may produce myoclonic jerks and coma. Later, if the patient has recovered, dementia, visual agnosia, choreoathetosis, and ataxia may occur.
Multiple sclerosis
This disorder rarely produces generalized seizures. Characteristic findings include vision deficits, paresthesia, constipation, muscle weakness, paralysis, spasticity, hyperreflexia, intention tremor, ataxic gait, dysphagia, dysarthria, impotence, and emotional lability. Urinary frequency, urgency, and incontinence may also occur.
Neurofibromatosis
Multiple brain lesions from this disorder cause focal and generalized seizures. Inspection reveals café-au-lait spots, multiple skin tumors, scoliosis, and kyphoscoliosis. Related findings include dizziness, ataxia, monocular blindness, and nystagmus.
Porphyria (intermittent acute)
Generalized seizures are a late sign of this disorder, indicating severe CNS involvement. Acute porphyria also causes severe abdominal pain, tachycardia, psychotic behavior, muscle weakness, and sensory loss in the trunk.
Sarcoidosis
Lesions may affect the brain, causing generalized and focal seizures. Associated findings include a nonproductive cough with dyspnea, substernal pain, malaise, fatigue, arthralgia, myalgia, weight loss, tachypnea, dysphagia, skin lesions, and impaired vision.
Stroke
Seizures (focal more often than generalized) may occur within 6 months of an ischemic stroke. Associated signs and symptoms vary with the location and extent of brain damage. They include decreased LOC, contralateral hemiplegia, dysarthria, dysphagia, ataxia, unilateral sensory loss, apraxia, agnosia, and aphasia. The patient may also develop visual deficits, memory loss, poor judgment, personality changes, emotional lability, urine retention or urinary incontinence, constipation, headache, and vomiting.
Other causes
Arsenic poisoning
Besides generalized seizures, arsenic poisoning may cause a garlicky breath odor, increased salivation, and generalized pruritus. GI effects include diarrhea, nausea, vomiting, and severe abdominal pain. Related effects include diffuse hyperpigmentation; sharply defined edema of the eyelids, face, and ankles; paresthesia of the extremities; alopecia; irritated mucous membranes; weakness; muscle aches; and peripheral neuropathy.
Barbiturate withdrawal
In chronically intoxicated patients, barbiturate withdrawal may produce generalized seizures 2 to 4 days after the last dose. Status epilepticus is possible.
Diagnostic tests
Contrast agents used in radiologic tests may cause generalized seizures.
Drugs
Toxic blood levels of some drugs, such as theophylline, lidocaine, meperidine, penicillins, and cimetidine, may cause generalized seizures. Phenothiazines, tricyclic antidepressants, amphetamines, isoniazid, and vincristine may cause seizures in patients with preexisting epilepsy.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006
Seizures, simple partial:
Medical causes
(Professional Guide to Signs & Symptoms (Fifth Edition))
Brain abscess
Seizures can occur in the acute stage of abscess formation or after resolution of the abscess. Decreased LOC varies from drowsiness to deep stupor. Early signs and symptoms reflect increased intracranial pressure and include a constant, intractable headache, nausea, and vomiting. Later signs and symptoms include ocular disturbances, such as nystagmus, decreased visual acuity, and unequal pupils. Other findings vary according to the abscess site and may include aphasia, hemiparesis, and personality changes.
Brain tumor
Focal seizures are commonly the earliest indicators of a brain tumor. The patient may report morning headache, dizziness, confusion, vision loss, and motor and sensory disturbances. He may also develop aphasia, generalized seizures, ataxia, decreased LOC, papilledema, vomiting, increased systolic blood pressure, and widening pulse pressure. Eventually, he may assume a decorticate posture.
Head trauma
Any head injury can cause seizures, but penetrating wounds are characteristically associated with focal seizures. The seizures usually begin 3 to 15 months after injury, decrease in frequency after several years, and eventually stop. The patient may develop generalized seizures and a decreased LOC that may progress to coma.
Multiple sclerosis
Focal or generalized seizures may occur with this disorder, usually during the late stages. Other findings include visual deficits, paresthesia, constipation, muscle weakness, spasticity, paralysis, hyperreflexia, intention tremor, gait ataxia, dysphagia, dysarthria, emotional lability, impotence, and urinary frequency, urgency, and incontinence.
Neurofibromatosis
Multiple brain lesions cause focal seizures and, at times, generalized seizures. Inspection reveals café-au-lait spots, multiple skin tumors, scoliosis, and kyphoscoliosis. Related findings include dizziness, ataxia, progressive monocular blindness, nystagmus, and endocrine abnormalities.
Sarcoidosis
Multiple lesions from this disorder affect the brain, producing focal and generalized seizures. Associated findings include a nonproductive cough with dyspnea, substernal pain, malaise, fatigue, arthralgia, myalgia, weight loss, tachypnea, dysphagia, skin lesions, and impaired vision.
Stroke
A major cause of seizures in patients older than age 50, a stroke may induce focal seizures up to 6 months after its onset. Related effects depend on the type and extent of the stroke but may include decreased LOC, contralateral hemiplegia, dysarthria, dysphagia, ataxia, unilateral sensory loss, apraxia, agnosia, and aphasia. A stroke may also cause visual deficits, memory loss, poor judgment, personality changes, emotional lability, headache, urinary incontinence or retention, and vomiting. It may result in generalized seizures.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Signs & Symptoms (Fifth Edition), 2006
Seizures:
Differential Overview
(Field Guide to Bedside Diagnosis)
❑ Generalized (grand mal)
❑ Partial (focal)
❑ Complex partial (temporal lobe)
❑ Absence (petit mal)
❑ Vasovagal syncope
❑ Myoclonic
❑ Akinetic (drop attacks)
❑ Psychomotor
❑ Pseudoseizures
» READ BOOK EXCERPT ONLINE »
Source: Field Guide to Bedside Diagnosis, 2007
Seizures, generalized tonic-clonic:
Medical causes
(Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series)
Alcohol withdrawal syndrome
Seizures as well as status epilepticus may develop 7 to 48 hours after abrupt cessation of alcohol consumption by the individual with alcohol dependency. Restlessness, hallucinations, profuse diaphoresis, and tachycardia may also occur.
Brain abscess
Generalized seizures may occur in the acute stage of abscess formation or after the abscess disappears. Decreased level of consciousness (LOC) varies from drowsiness to deep stupor according to the size and location of the abscess. Early signs and symptoms reflect increased intracranial pressure (ICP) and include constant headache, nausea, vomiting, and focal seizures. Typical later features include ocular disturbances, such as nystagmus, impaired vision, and unequal pupils. Other findings vary with the abscess site, but may include aphasia, hemiparesis, abnormal behavior, and personality changes.
Brain tumor
Generalized seizures may occur, depending on the tumor’s location and type. Other findings include a slowly decreasing LOC, morning headache, dizziness, confusion, focal seizures, vision loss, motor and sensory disturbances, aphasia, and ataxia. Later findings include papilledema, vomiting, increased systolic blood pressure, widening pulse pressure and, eventually, decorticate posture.
Cerebral aneurysm
Occasionally, generalized seizures may occur with an aneurysm rupture. Premonitory signs and symptoms may last several days, but the onset is typically abrupt with severe headache, nausea, vomiting, and a decreased LOC. Related signs and symptoms vary according to the site and amount of bleeding, but may include nuchal rigidity, irritability, hemiparesis, hemisensory defects, dysphagia, photophobia, diplopia, ptosis, and unilateral pupil dilation.
Chronic renal failure
End-stage renal failure produces the rapid onset of twitching, trembling, myoclonic jerks, and generalized seizures. Related signs and symptoms include anuria or oliguria, fatigue, malaise, irritability, decreased mental acuity, muscle cramps, peripheral neuropathies, anorexia, and constipation or diarrhea. Integumentary effects include skin color changes (yellow, brown, or bronze), pruritus, and uremic frost. Other effects include ammonia breath odor, nausea and vomiting, ecchymoses, petechiae, GI bleeding, mouth and gum ulcers, hypertension, and Kussmaul’s respirations.
Eclampsia
Generalized seizures are a hallmark of eclampsia. Related findings include severe frontal headache, nausea and vomiting, vision disturbances, increased blood pressure, fever of up to 104° (40° C), peripheral edema, and sudden weight gain. The patient may also exhibit oliguria, irritability, hyperactive deep tendon reflexes (DTRs), and a decreased LOC.
Encephalitis
Seizures are an early sign of encephalitis, indicating a poor prognosis; they may also occur after recovery as a result of residual damage. Other findings include fever, headache, photophobia, nuchal rigidity, neck pain, vomiting, aphasia, ataxia, hemiparesis, nystagmus, irritability, cranial nerve palsies (causing facial weakness, ptosis, and dysphagia), and myoclonic jerks.
Epilepsy (idiopathic)
In most cases, the cause of recurrent seizures is unknown.
Head trauma
In severe cases, generalized seizures may occur at the time of injury. (Months later, focal seizures may occur.) Severe head trauma may also cause a decreased LOC, leading to coma. Other signs and symptoms may include soft-tissue injury of the face, head, or neck as well as facial edema and clear or bloody drainage from the mouth, nose, or ears. The patient may also exhibit Battle’s sign, lack of response to oculocephalic and oculovestibular stimulation, and bony deformity of the face, head, or neck. Motor and sensory deficits may occur along with altered respirations. Examination may reveal signs of increasing ICP, such as decreased response to painful stimuli, nonreactive pupils, bradycardia, increased systolic pressure, and widening pulse pressure. If the patient is conscious, he may exhibit visual deficits, behavioral changes, and headache.
Hepatic encephalopathy
Generalized seizures may occur late in hepatic encephalopathy. Associated late-stage findings in the comatose patient include fetor hepaticus, asterixis, hyperactive DTRs, and a positive Babinski’s sign.
Hypertensive encephalopathy
A life-threatening disorder, hypertensive encephalopathy may cause seizures along with severely increased blood pressure, a decreased LOC, intense headache, vomiting, transient blindness, paralysis and, eventually, Cheyne-Stokes respirations.
Hypoglycemia
Generalized seizures usually occur with severe hypoglycemia, accompanied by blurred or double vision, motor weakness, hemiplegia, trembling, excessive diaphoresis, tachycardia, myoclonic twitching, and a decreased LOC.
Hyponatremia
Seizures develop when serum sodium levels fall below 125 mEq/L, especially if the decrease is rapid. Hyponatremia also causes orthostatic hypotension, headache, muscle twitching and weakness, fatigue, oliguria or anuria, cold and clammy skin, decreased skin turgor, irritability, lethargy, confusion, and stupor or coma. Excessive thirst, tachycardia, nausea, vomiting, and abdominal cramps may also occur. Severe hyponatremia may cause cyanosis and vasomotor collapse, with a thready pulse.
Hypoparathyroidism
Worsening tetany causes generalized seizures. Chronic hypoparathyroidism produces neuromuscular irritability and hyperactive DTRs.
Hypoxic encephalopathy
Besides generalized seizures, hypoxic encephalopathy may produce myoclonic jerks and coma. Later, if the patient has recovered, dementia, visual agnosia, choreoathetosis, and ataxia may occur.
Multiple sclerosis (MS)
MS rarely produces generalized seizures. Characteristic findings include vision deficits, paresthesia, constipation, muscle weakness, paralysis, spasticity, hyperreflexia, intention tremor, ataxic gait, dysphagia, dysarthria, impotence, and emotional lability. Urinary frequency, urgency, and incontinence may also occur.
Neurofibromatosis
Multiple brain lesions from neurofibromatosis cause focal and generalized seizures. Inspection reveals café-au-lait spots, multiple skin tumors, scoliosis, and kyphoscoliosis. Related findings include dizziness, ataxia, monocular blindness, and nystagmus.
Porphyria (intermittent acute)
Generalized seizures are a late sign of porphyria, indicating severe CNS involvement. Acute porphyria also causes severe abdominal pain, tachycardia, psychotic behavior, muscle weakness, and sensory loss in the trunk.
Sarcoidosis
Lesions may affect the brain, causing generalized and focal seizures. Associated findings include a nonproductive cough with dyspnea, substernal pain, malaise, fatigue, arthralgia, myalgia, weight loss, tachypnea, dysphagia, skin lesions, and impaired vision.
Stroke
Seizures (focal more common than generalized) may occur within 6 months of an ischemic stroke. Associated signs and symptoms vary with the location and extent of brain damage. They include a decreased LOC, contralateral hemiplegia, dysarthria, dysphagia, ataxia, unilateral sensory loss, apraxia, agnosia, and aphasia. The patient may also develop visual deficits, memory loss, poor judgment, personality changes, emotional lability, urine retention or urinary incontinence, constipation, headache, and vomiting.
Other causes
Arsenic poisoning
Besides generalized seizures, arsenic poisoning may cause a garlicky breath odor, increased salivation, and generalized pruritus. GI effects include diarrhea, nausea, vomiting, and severe abdominal pain. Related effects include diffuse hyperpigmentation, paresthesia of the extremities, alopecia, irritated mucous membranes, weakness, muscle aches, peripheral neuropathy, and sharply defined edema of the eyelids, face, and ankles.
Barbiturate withdrawal
In chronically intoxicated patients, barbiturate withdrawal may produce generalized seizures 2 to 4 days after the last dose. Status epilepticus is possible.
Diagnostic tests
Contrast agents used in radiologic tests may cause generalized seizures.
Drugs
Toxic blood levels of some drugs, such as theophylline, lidocaine, Indocin, meperidine, penicillins, and cimetidine, may cause generalized seizures. Phenothiazines, tricyclic antidepressants, amphetamines, isoniazid, and vincristine may cause seizures in patients with preexisting epilepsy.
» READ BOOK EXCERPT ONLINE »
Source: Alarming Signs and Symptoms: Lippincott Manual of Nursing Practice Series, 2007
Seizures, complex partial:
Medical causes
(Signs & Symptoms: A 2-in-1 Reference for Nurses)
Brain abscess
If the brain abscess is in the temporal lobe, complex partial seizures commonly occur after the abscess disappears. Related problems may include headache, nausea, vomiting, generalized seizures, and a decreased level of consciousness (LOC). The patient may also develop central facial weakness, auditory receptive aphasia, hemiparesis, and ocular disturbances.
Head trauma
Severe trauma to the temporal lobe (especially from a penetrating injury) can produce complex partial seizures months or years later. The seizures may decrease in frequency and eventually stop. Head trauma also causes generalized seizures and behavior and personality changes.
Temporal lobe tumor
Complex partial seizures may be the first sign of a tumor in the temporal lobe. Other signs and symptoms include headache, pupillary changes, and mental dullness. Increased intracranial pressure may cause a decreased LOC, vomiting and, possibly, papilledema.
» READ BOOK EXCERPT ONLINE »
Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007
Seizures, generalized tonic-clonic:
Medical causes
(Signs & Symptoms: A 2-in-1 Reference for Nurses)
Alcohol withdrawal syndrome
Sudden withdrawal from alcohol dependence may cause seizures 7 to 48 hours later as well as status epilepticus. The patient may also be restless and exhibit hallucinations, profuse diaphoresis, and tachycardia.
Arsenic poisoning
Besides generalized seizures, arsenic poisoning may cause a garlicky breath odor, increased salivation, and generalized pruritus. GI effects include diarrhea, nausea, vomiting, and severe abdominal pain. Related effects include diffuse hyperpigmentation; sharply defined edema of the eyelids, face, and ankles; paresthesia of the extremities; alopecia; irritated mucous membranes; weakness; muscle aches; and peripheral neuropathy.
Brain abscess
Generalized seizures may occur in the acute stage of abscess formation or after the abscess disappears. Depending on the size and location of the abscess, decreased level of consciousness (LOC) varies from drowsiness to deep stupor. Early signs and symptoms reflect increased intracranial pressure (ICP) and include constant headache, nausea, vomiting, and focal seizures. Typical later features include ocular disturbances, such as nystagmus, impaired vision, and unequal pupils. Other findings vary with the abscess site but may include aphasia, hemiparesis, abnormal behavior, and personality changes.
Brain tumor
Generalized seizures may occur, depending on the tumor’s location and type. Other findings include a slowly decreasing LOC, morning headache, dizziness, confusion, focal seizures, vision loss, motor and sensory disturbances, aphasia, and ataxia. Later findings include papilledema, vomiting, increased systolic blood pressure, widening pulse pressure, and (eventually) decorticate posture.
Cerebral aneurysm
Occasionally, generalized seizures may occur with an aneurysmal rupture. Premonitory signs and symptoms may last several days, but onset is typically abrupt with severe headache, nausea, vomiting, and decreased LOC. Depending on the site and amount of bleeding, related signs and symptoms vary but may include nuchal rigidity, irritability, hemiparesis, hemisensory defects, dysphagia, photophobia, diplopia, ptosis, and unilateral pupil dilation.
Eclampsia
Generalized seizures are a hallmark of eclampsia. Related findings include severe frontal headache, nausea and vomiting, vision disturbances, increased blood pressure, fever of up to 104° F (40° C), peripheral edema, and sudden weight gain. The patient may also exhibit oliguria, irritability, hyperactive deep tendon reflexes (DTRs), and decreased LOC.
Encephalitis
Seizures are an early sign of encephalitis, indicating a poor prognosis; they may also occur after recovery as a result of residual damage. Other findings include fever, headache, photophobia, nuchal rigidity, neck pain, vomiting, aphasia, ataxia, hemiparesis, nystagmus, irritability, cranial nerve palsies (causing facial weakness, ptosis, dysphagia), and myoclonic jerks.
Head trauma
In severe cases, generalized seizures may occur at the time of injury. (Months later, focal seizures may occur.) Severe head trauma may also cause a decreased LOC, leading to coma; soft-tissue injury of the face, head, or neck; clear or bloody drainage from the mouth, nose, or ears; facial edema; bony deformity of the face, head, or neck; Battle’s sign; and lack of response to oculocephalic and oculovestibular stimulation. Motor and sensory deficits may occur along with altered respirations. Examination may reveal signs of increasing ICP, such as decreased response to painful stimuli, nonreactive pupils, bradycardia, increased systolic pressure, and widening pulse pressure. If the patient is conscious, he may exhibit vision deficits, behavioral changes, and headache.
Hepatic encephalopathy
Generalized seizures may occur late in hepatic encephalopathy. Associated late-stage findings in the comatose patient include fetor hepaticus, asterixis, hyperactive DTRs, and a positive Babinski’s sign.
Hypertensive encephalopathy
Hypertensive encephalopathy, a life-threatening disorder, may cause seizures along with severely increased blood pressure, decreased LOC, intense headache, vomiting, transient blindness, paralysis, and (eventually) Cheyne-Stokes respirations.
Hypoglycemia
Generalized seizures usually occur with severe hypoglycemia, accompanied by blurred or double vision, motor weakness, hemiplegia, trembling, excessive diaphoresis, tachycardia, myoclonic twitching, and decreased LOC.
Hyponatremia
Seizures develop when serum sodium levels fall below 125 mEq/L, especially if the decrease is rapid. Hyponatremia also causes orthostatic hypotension, headache, muscle twitching and weakness, fatigue, oliguria or anuria, cold and clammy skin, decreased skin turgor, irritability, lethargy, confusion, and stupor or coma. Excessive thirst, tachycardia, nausea, vomiting, and abdominal cramps may also occur. Severe hyponatremia may cause cyanosis and vasomotor collapse, with a thready pulse.
Hypoparathyroidism
Worsening tetany causes generalized seizures. Chronic hypoparathyroidism produces neuromuscular irritability, Chvostek’s sign, dysphagia, tetany, and hyperactive DTRs.
Hypoxic encephalopathy
Besides generalized seizures, hypoxic encephalopathy may produce myoclonic jerks and coma. Later, if the patient has recovered, dementia, visual agnosia, choreoathetosis, and ataxia may occur.
Neurofibromatosis
Multiple brain lesions from neurofibromatosis cause focal and generalized seizures. Inspection reveals café-au-lait spots, multiple skin tumors, scoliosis, and kyphoscoliosis. Related findings include dizziness, ataxia, monocular blindness, and nystagmus.
Renal failure (chronic)
End-stage renal failure produces rapid onset of twitching, trembling, myoclonic jerks, and generalized seizures. Related signs and symptoms include anuria or oliguria, fatigue, malaise, irritability, decreased mental acuity, muscle cramps, peripheral neuropathies, anorexia, and constipation or diarrhea. Integumentary effects include skin color changes (yellow, brown, or bronze), pruritus, and uremic frost. Other effects include ammonia breath odor, nausea and vomiting, ecchymoses, petechiae, GI bleeding, mouth and gum ulcers, hypertension, and Kussmaul’s respirations.
Stroke
Seizures (focal more often than generalized) may occur within 6 months of an ischemic stroke. Associated signs and symptoms vary with the location and extent of brain damage. They include decreased LOC, contralateral hemiplegia, dysarthria, dysphagia, ataxia, unilateral sensory loss, apraxia, agnosia, and aphasia. The patient may also develop visual deficits, memory loss, poor judgment, personality changes, emotional lability, urine retention or urinary incontinence, constipation, headache, and vomiting.
Other causes
Barbiturate withdrawal
In chronically intoxicated patients, barbiturate withdrawal may produce generalized seizures 2 to 4 days after the last dose. Status epilepticus is possible.
Diagnostic tests
Contrast agents used in radiologic tests may cause generalized seizures.
Drugs
Toxic blood levels of some drugs, such as theophylline, lidocaine, meperidine, penicillins, and cimetidine, may cause generalized seizures. Phenothiazines, tricyclic antidepressants, amphetamines, isoniazid, and vincristine may cause seizures in patients with preexisting epilepsy.
» READ BOOK EXCERPT ONLINE »
Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007
Seizures, simple partial:
Medical causes
(Signs & Symptoms: A 2-in-1 Reference for Nurses)
Brain abscess
Seizures can occur in the acute stage of abscess formation or after resolution of the abscess. Decreased LOC varies from drowsiness to deep stupor. Early signs and symptoms reflect increased intracranial pressure and include a constant, intractable headache, nausea, and vomiting. Later signs and symptoms include ocular disturbances, such as nystagmus, decreased visual acuity, and unequal pupils. Other findings vary according to the abscess site and may include aphasia, hemiparesis, and personality changes.
Brain tumor
Focal seizures are commonly the earliest indicators of a brain tumor. The patient may report morning headache, dizziness, confusion, vision loss, and motor and sensory disturbances. He may also develop aphasia, generalized seizures, ataxia, decreased LOC, papilledema, vomiting, increased systolic blood pressure, and widening pulse pressure. Eventually, he may assume a decorticate posture.
Head trauma
Any head injury can cause seizures, but penetrating wounds are characteristically associated with focal seizures. The seizures usually begin 3 to 15 months after injury, decrease in frequency after several years, and eventually stop. The patient may develop generalized seizures and a decreased LOC that may progress to coma.
Multiple sclerosis
Focal or generalized seizures may occur with multiple sclerosis, usually during the late stages. Other findings include visual deficits, paresthesia, constipation, muscle weakness, spasticity, paralysis, hyperreflexia, intention tremor, gait ataxia, dysphagia, dysarthria, emotional lability, impotence, and urinary frequency, urgency, and incontinence.
Neurofibromatosis
With neurofibromatosis, multiple brain lesions cause focal seizures and, at times, generalized seizures. Inspection reveals café-au-lait spots, multiple skin tumors, scoliosis, and kyphoscoliosis. Related findings include dizziness, ataxia, progressive monocular blindness, nystagmus, and endocrine abnormalities.
Stroke
A major cause of seizures in patients older than age 50, a stroke may induce focal seizures up to 6 months after its onset. Related effects depend on the type and extent of the stroke but may include decreased LOC, contralateral hemiplegia, dysarthria, dysphagia, ataxia, unilateral sensory loss, apraxia, agnosia, and aphasia. A stroke may also cause vision deficits, memory loss, poor judgment, personality changes, emotional lability, headache, urinary incontinence or retention, and vomiting. It may result in generalized seizures.
» READ BOOK EXCERPT ONLINE »
Source: Signs & Symptoms: A 2-in-1 Reference for Nurses, 2007
Seizures:
Principal Causes of Seizures
(The Diagnostic Approach to Symptoms and Signs in Pediatrics)
- Febrileseizures
- Hypoxic-ischemic encephalopathy
- Brain disorders
- Cerebralmalformations
- Intracranial infection
- Intracranial hemorrhage
- Other
- Hypertensive encephalopathy
- Drugs and toxins
- Metabolic disorders
- Hypoglycemia
- Hypocalcemia
- Hypomagnesemia
- Hyponatremia
- Hypernatremia
- Uremia
- Bilirubin encephalopathy (kernicterus)
- Pyridoxine dependency
- Inborn errors of metabolism
- Selected epileptic syndromes
- Neonatalseizures
- Benign neonatal epilepsy
- Infantile spasms (West syndrome)
- Lennox-Gastaut syndrome
- Benign focal epilepsy with centrotemporalspikes
- Temporal lobe epilepsy
- Juvenile myoclonic epilepsy
- Posttraumatic epilepsy
- Childhood absence epilepsy
- Unknown
» READ BOOK EXCERPT ONLINE »
Source: The Diagnostic Approach to Symptoms and Signs in Pediatrics, 2006
Seizures, absence:
Medical causes
(Nursing: Interpreting Signs and Symptoms)
Idiopathic epilepsy.Some forms of absence seizure are accompanied by learning disabilities.
Other causes
Drugs.Drugs that lower the threshold for seizures, such as alcohol, cocaine, penicillin in high doses, isoniazid, and phenothiazines may trigger seizures in patients with preexisting epilepsy.
» READ BOOK EXCERPT ONLINE »
Source: Nursing: Interpreting Signs and Symptoms, 2007
Seizures, complex partial:
Medical causes
(Nursing: Interpreting Signs and Symptoms)
Brain abscess.If the brain abscess is in the temporal lobe, complex partial seizures commonly occur after the abscess disappears. Related problems may include headache, nausea, vomiting, generalized seizures, and decreased level of consciousness (LOC). The patient may also develop central facial weakness, auditory receptive aphasia, hemiparesis, and ocular disturbances.
Head trauma.Severe trauma to the temporal lobe (especially from a penetrating injury) can produce complex partial seizures months or years later. The seizures may decrease in frequency and eventually stop. Head trauma also causes generalized seizures and behavior and personality changes.
Herpes simplex encephalitis.Herpes simplex virus commonly attacks the temporal lobe, resulting in complex partial seizures. Other features include fever, headache, coma, and generalized seizures.
Temporal lobe tumor.Complex partial seizures may be the first sign of a temporal lobe tumor. Other signs and symptoms include headache, pupillary changes, and mental dullness. Increased intracranial pressure may cause decreased LOC, vomiting and, possibly, papilledema.
» READ BOOK EXCERPT ONLINE »
Source: Nursing: Interpreting Signs and Symptoms, 2007
Seizures, generalized tonic-clonic:
Medical causes
(Nursing: Interpreting Signs and Symptoms)
Brain abscess.Generalized seizures may occur in the acute stage of a brain abscess formation or after the abscess disappears. Depending on the size and location of the abscess, a decreased LOC varies from drowsiness to deep stupor. Early signs and symptoms reflect increased intracranial pressure (ICP) and include a constant headache, nausea, vomiting, and focal seizures. Typical later features include ocular disturbances, such as nystagmus, impaired vision, and unequal pupils. Other findings vary with the abscess site but may include aphasia, hemiparesis, abnormal behavior, and personality changes.
Brain tumor.Generalized seizures may occur with a brain tumor, depending on it's location and type. Other findings include a slowly decreasing LOC, a morning headache, dizziness, confusion, focal seizures, vision loss, motor and sensory disturbances, aphasia, and ataxia. Later findings include papilledema, vomiting, increased systolic blood pressure, widening pulse pressure and, eventually, a decorticate posture.
Chronic renal failure.End-stage renal failure produces the rapid onset of twitching, trembling, myoclonic jerks, and generalized seizures. Related signs and symptoms include anuria or oliguria, fatigue, malaise, irritability, decreased mental acuity, muscle cramps, peripheral neuropathies, anorexia, and constipation or diarrhea. Integumentary effects include skin color changes (yellow, brown, or bronze), pruritus, and uremic frost. Other effects include an ammonia breath odor, nausea and vomiting, ecchymoses, petechiae, GI bleeding, mouth and gum ulcers, hypertension, and Kussmaul's respirations.
Eclampsia.Generalized seizures are a hallmark of eclampsia. Related findings include a severe frontal headache, nausea and vomiting, vision disturbances, increased blood pressure, a fever of up to 104° F (40° C), peripheral edema, and sudden weight gain. The patient may also exhibit oliguria, irritability, hyperactive deep tendon reflexes (DTRs), and decreased LOC.
Encephalitis.Seizures are an early sign of encephalitis, indicating a poor prognosis; they may also occur after recovery as a result of residual damage. Other findings include fever, headache, photophobia, nuchal rigidity, neck pain, vomiting, aphasia, ataxia, hemiparesis, nystagmus, irritability, cranial nerve palsies (causing facial weakness, ptosis, and dysphagia), and myoclonic jerks.
Epilepsy (idiopathic).In most cases, the cause of recurrent seizures is unknown.
Head trauma.With severe head trauma, generalized seizures may occur at the time of injury. (Months later, focal seizures may occur.) Severe head trauma may also cause decreased LOC, leading to coma; soft-tissue injury of the face, head, or neck; clear or bloody drainage from the mouth, nose, or ears; facial edema; bony deformity of the face, head, or neck; Battle's sign; and a lack of response to oculocephalic and oculovestibular stimulation. Motor and sensory deficits may occur along with altered respirations. Examination may reveal signs of increasing ICP, such as a decreased response to painful stimuli, nonreactive pupils, bradycardia, increased systolic pressure, and widening pulse pressure. If the patient is conscious, he may exhibit visual deficits, behavioral changes, and headache.
Hepatic encephalopathy.Generalized seizures may occur latein hepatic encephalopathy. Associated late-stage findings in the comatose patient include fetor hepaticus, asterixis, hyperactive DTRs, and a positive Babinski's sign.
Hypoglycemia.Generalized seizures usually occur with severe hypoglycemia, accompanied by blurred or double vision, motor weakness, hemiplegia, trembling, excessive diaphoresis, tachycardia, myoclonic twitching, and decreased LOC.
Hyponatremia.Seizures may develop when the serum sodium level falls below 125 mEq/L, especially if the sodium loss is rapid. Hyponatremia also causes orthostatic hypotension, headache, muscle twitching and weakness, fatigue, oliguria or anuria, cold and clammy skin, decreased skin turgor, irritability, lethargy, confusion, and stupor or coma. Excessive thirst, tachycardia, nausea, vomiting, and abdominal cramps may also occur. Severe hyponatremia may cause cyanosis and vasomotor collapse, with a thready pulse.
Hypoparathyroidism.Chronic hypoparathyroidism produces neuromuscular irritability and hyperactive DTRs. Worsening tetany causes generalized seizures.
Hypoxic encephalopathy.Besidesgeneralized seizures, hypoxic encephalopathy may produce myoclonic jerks and coma. Later, if the patient has recovered, dementia, visual agnosia, choreoathetosis, and ataxia may occur.
Neurofibromatosis.Multiple brain lesions from neurofibromatosis cause focal and generalized seizures. Inspection reveals café-au-lait spots, multiple skin tumors, scoliosis, and kyphoscoliosis. Related findings include dizziness, ataxia, monocular blindness, and nystagmus.
Stroke.Seizures (focal more commonly than generalized) may occur within 6 months of an ischemic stroke. Associated signs and symptoms vary with the location and extent of brain damage. They include decreased LOC, contralateral hemiplegia, dysarthria, dysphagia, ataxia, unilateral sensory loss, apraxia, agnosia, and aphasia. The patient may also develop visual deficits, memory loss, poor judgment, personality changes, emotional lability, urine retention or urinary incontinence, constipation, headache, and vomiting.
Other causes
Arsenic poisoning.Besides generalized seizures, arsenic poisoning may cause a garlicky breath odor, increased salivation, and generalized pruritus. GI effects include diarrhea, nausea, vomiting, and severe abdominal pain. Related effects include diffuse hyperpigmentation; sharply defined edema of the eyelids, face, and ankles; paresthesia of the extremities; alopecia; irritated mucous membranes; weakness; muscle aches; and peripheral neuropathy.
Barbiturate withdrawal.In chronically intoxicated patients, barbiturate withdrawal may produce generalized seizures 2 to 4 days after the last dose. Status epilepticus is possible.
Diagnostic tests.Contrast agents used in radiologic tests may cause generalized seizures.
Drugs.Toxic blood levels of some drugs, such as theophylline, lidocaine, meperidine, penicillins, and cimetidine, may cause generalized seizures. Phenothiazines, tricyclic antidepressants, amphetamines, isoniazid, and vincristine may cause seizures in patients with preexisting epilepsy.
» READ BOOK EXCERPT ONLINE »
Source: Nursing: Interpreting Signs and Symptoms, 2007
Seizures, simple partial:
Medical causes
(Nursing: Interpreting Signs and Symptoms)
Brain abscess.Seizures can occur in the acute stage of a brain abscess formation or after resolution of the abscess. A decreased LOC varies from drowsiness to deep stupor. Early signs and symptoms reflect increased intracranial pressure and include a constant, intractable headache; nausea; and vomiting. Later signs and symptoms include ocular disturbances, such as nystagmus, decreased visual acuity, and unequal pupils. Other findings vary according to the abscess site and may include aphasia, hemiparesis, and personality changes.
Brain tumor.Focal seizures are commonly the earliest indicators of a brain tumor. The patient may report a morning headache, dizziness, confusion, vision loss, and motor and sensory disturbances. He may also develop aphasia, generalized seizures, ataxia, decreased LOC, papilledema, vomiting, increased systolic blood pressure, and widening pulse pressure. Eventually, he may assume a decorticate posture.
Head trauma.Any head injury can cause seizures, but penetrating wounds are characteristically associated with focal seizures. The seizures usually begin 3 to 15 months after injury, decrease in frequency after several years, and eventually stop. The patient may develop generalized seizures and decreased LOC that may progress to coma.
Stroke.A major cause of seizures, a stroke may induce focal seizures up to 6 months after its onset. Related effects depend on the type and extent of the stroke, but may include decreased LOC, contralateral hemiplegia, dysarthria, dysphagia, ataxia, unilateral sensory loss, apraxia, agnosia, and aphasia. A stroke may also cause visual deficits, memory loss, poor judgment, personality changes, emotional lability, headache, urinary incontinence or urine retention, and vomiting. It may result in generalized seizures.
» READ BOOK EXCERPT ONLINE »
Source: Nursing: Interpreting Signs and Symptoms, 2007
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