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Common causes of Speech symptoms
Introduction:
This information shows the various causes of Speech symptoms, and how common these diseases or conditions are in the general population. This is not a direct indication as to how commonly these diseases are the actual cause of Speech symptoms, but gives a relative idea as to how frequent these diseases are seen overall.
Causes of Speech symptoms that are very common
The following causes of Speech symptoms are diseases or medical conditions that affect more than 10 million people in the USA:
- Alcohol abuse - slurred speech
- Asthma - difficulty speaking
- Migraine - speech difficulty
- Social phobia - difficulty talking
Causes of Speech symptoms that are common
The following causes of Speech symptoms are diseases or conditions that affect more than 1 million people in the USA:
- Alzheimer's Disease - loss of speech
- Aphasia - jumbled speech
- Attention Deficit Hyperactivity Disorder - talking too much
- Bipolar disorder - excessive talkativeness
- Parkinson's Disease - speech changes
- Sjogren's Syndrome - speaking difficulty
- Stroke - speech problems
Causes of Speech symptoms that are uncommon
The following causes of Speech symptoms are diseases or conditions that affect more than 200,000 people, but less than 1 million people in the USA:
- Autism - No gesturing by 12 months
- Cerebral Palsy - speech difficulty
- Cleft palate - speech defects
- Klinefelter syndrome - speech difficulty
- Multiple Sclerosis - slurred speech
- Nonaffective Psychosis - Speech difficulties
Causes of Speech symptoms that are rare
The offical US government definition of a "rare" disease is one that affects 200,000 people or less. The following causes of Speech symptoms appear in the population at a rate of less than 200,000 people per year in the USA:
- Alexander Syndrome - speech abnormalities
- Ataxia Telangiectasia - slurred speech
- Behcet's Disease - impaired speech
- Binswanger's Disease - speech difficulties
- Coffin-Lowry syndrome - speech retardation
- Fahr's Syndrome - dysarthria (poorly articulated speech)
- Hallervorden-Spatz disease - dysarthria
- Landau-Kleffner Syndrome - aphasia
- Machado-Joseph Disease - speech difficulty
- Mobius syndrome - speech difficulties
- Moyamoya Disease - speech deficits (aphasia)
- Narcolepsy - slurred speech
- Pelizaeus-Merzbacher Disease - deteriorating speech
- Primary Lateral Sclerosis - dysarthria (poorly articulated speech)
- Progressive Supranuclear Palsy - speech difficulties
- Rasmussen's Encephalitis - speech deficits
- Schilder's Disease - speech impairment
- Soto's Syndrome - speech impairment
Causes of Speech symptoms that are very rare
The following causes of Speech symptoms appear in the population at a rate of substantially less than 200,000 people per year in the USA:
- Amyotrophic lateral sclerosis - difficulty speaking
- Bell's Palsy - difficulting speaking
- Botulism food poisoning - speech difficulty
- Brain cancer - speech problems
- Creutzfeldt-Jakob Disease - speaking difficulty
- East African Trypanosomiasis - difficulty talking
- Fetal alcohol syndrome - speech impairment
- Fragile-X Syndrome - cluttered speech
- Huntington's Disease - slurred speech
- Motor neuron diseases - slurred speech
- Myasthenia Gravis - difficulty talking
- Porencephaly - speech problems
- Rabies - change in phonation
- Schizencephaly - speech delay
- Thyroid cancer - difficulty speaking
- Trichinosis - difficulty speaking
- Usher Syndrome - speech problems
- Velocardiofacial syndrome - delayed speech development
- Western equine encephalitis - Aphasia
Causes of Speech symptoms without any prevalence information
The following causes of Speech symptoms are ones for which we do not have any prevalence information.
- 1q deletion - speech retardation
- 3-methylglutaconic aciduria, type 1 - speech delay
- 3C syndrome - speech defect
- 3q deletion - speech retardation
- Aarskog-Ose-Pande syndrome - delayed speech development
- Aceruloplasminemia - dysarthria
- Acrofacial dysostosis, Nager type - delayed speech development
- Acromesomelic dysplasia Hunter Thompson type - speech defect
- Adenoid cystic carcinoma - speech changes
- Adrenoleukodystrophy - aphasia
- Adrenomyeloneuropathy - speech difficulties
- Adult SMA - difficulty speaking
- African Sleeping sickness - difficulty talking
- Albinism deafness syndrome - mutism
- Alcohol abuse - slurred speech
- Alcohol drinking - incoherent speech
- Alcohol-Induced Disorders - incoherent speech
- Allan-Herndon-Dudley Syndrome - speaking difficulty
- Alopecia - hypogonadism - extrapyramidal disorder - dysarthria
- Alport Syndrome - speech retardation
- Alzheimer disease 10 - speech problems
- Alzheimer disease 12 - speech problems
- Alzheimer disease 13 - speech problems
- Alzheimer disease 14 - speech problems
- Alzheimer disease 15 - speech problems
- Alzheimer disease 5 - speech problems
- Alzheimer disease 6 - speech problems
- Alzheimer disease 7 - speech problems
- Alzheimer disease 8 - speech problems
- Alzheimer disease 9 - speech problems
- Alzheimer disease type 1 - speech problems
- Alzheimer disease type 2 - speech problems
- Alzheimer disease type 4 - speech problems
- Alzheimer disease, familial - speech problems
- Alzheimer disease, familial, 1 - speech problems
- Alzheimer disease, familial, type 3 - speech problems
- Alzheimer's Disease - loss of speech
- Alzheimer's disease without Neurofibrillary tangles - speech problems
- Amphetamine abuse - talkative
- Ampola syndrome - speech defect
- Amyloidosis, oculoleptomeningeal - dysarthria
- Amyotrophic lateral sclerosis 3 - dysarthria
- Amyotrophic lateral sclerosis 6 - dysarthria
- Amyotrophic lateral sclerosis 7 - dysarthria
- Amyotrophic lateral sclerosis 8 - dysarthria
- Amyotrophic lateral sclerosis, familial type 1 - slurred speech
- Amyotrophic lateral sclerosis, familial type 2 - slurred speech
- Amyotrophic lateral sclerosis, familial type 3 - slurred speech
- Amyotrophic lateral sclerosis, familial type 4 - slurred speech
- Amyotrophic lateral sclerosis, familial type 5 - slurred speech
- Amyotrophic lateral sclerosis, familial type 6 - slurred speech
- Amyotrophic lateral sclerosis, familial type 7 - slurred speech
- Amyotrophic lateral sclerosis, familial type 8 - slurred speech
- Aneurysm, intracranial berry - speech impairment
- Aneurysm, intracranial berry, 1 - speech impairment
- Aneurysm, intracranial berry, 2 - speech impairment
- Aneurysm, intracranial berry, 3 - speech impairment
- Aneurysm, intracranial berry, 4 - speech impairment
- Aneurysm, intracranial berry, 5 - speech impairment
- Aneurysm, intracranial berry, 6 - speech impairment
- Aneurysm, intracranial berry, 7 - speech impairment
- Aneurysm, intracranial berry, 8 - speech impairment
- Angelman syndrome - absent speech
- Anton-Vogt syndrome - dysarthria
- Aphasia - jumbled speech
- Arnold Stickler Bourne syndrome - speech defect
- Arteriovenous Malformation - loss of speech
- Asperger syndrome - speech and language peculiarities
- Asthma - difficulty speaking
- Ataxia - difficulty pronouncing words
- Ataxia spastic congenital miosis - speech defect
- Ataxia, Hereditary, Autosomal Dominant - dysarthria
- Ataxia, spastic with congenital miosis - dysarthria
- Ataxia, spastic, 3, autosomal recessive - dysarthria
- Ataxia-oculomotor apraxia syndrome - dysarthria
- Auriculo-condylar syndrome - speech problems
- Babinski-Nageotte syndrome - dysarthria
- Bahemuka Brown syndrome - dysarthria
- Bannayan-Zonana syndrome - speech delay
- Barbiturate abuse - trouble talking
- Basal ganglia calcification, idiopathic 1 - dysarthria
- Basal ganglia disease, biotin-responsive - dysarthria
- Basilar artery migraine - dysarthria
- Bell's Palsy - difficulting speaking
- Benign astrocytoma - aphasia
- Benign essential tremor syndrome - speech impairment
- Brailsford - delayed talking
- Brain - bone - fat - speech defect
- Brain cancer - speech problems
- Brain Concussion - slurred speech
- Brain conditions - Dysarthria
- Brain tumor, adult - speaking difficulty
- Branchial arch syndrome X-linked - speech defect
- Bristowe's syndrome - loss of speech
- Brown-Vialetto-Van Laere syndrome - speech difficulty
- CACH syndrome - slurred speech
- Calcification of basal ganglia with or without hypocalcemia - speech problems
- CANOMAD syndrome - dysarthria
- Cardiomyopathy - hearing loss, type t RNA lysine gene mutation - slurred speech
- Carpenter syndrome - speech problems
- Catatonic syndrome - mutism
- Central pontine myelinolysis - speech problems
- Cerebellar abscess - speech difficulties
- Cerebellar ataxia syndrome - speaking difficulty
- Cerebellar ataxia type 1, autosomal recessive - dysarthria
- Cerebellar ataxia, autosomal recessive - dysarthria
- Cerebellar ataxia, infantile with progressive external ophthalmoplegia - speech difficulty
- Cerebellar ataxia, X-linked - dysarthria
- Cerebellar degeneration - slurred speech
- Cerebellar degeneration, subacute - dysarthria
- Cerebelloparenchymal autosomal recessive disorder 3 - speech defect
- Cerebral abscess - speech difficulties
- Cerebral Atrophy - speech impairment
- Cerebral hemorrhage - speech problems
- Cerebrocostomandibular Syndrome - speech difficulties
- Cerebrorenodigital syndrome - speech defect
- Cerebrovascular accident - difficulty talking or swallowing
- Ceroid lipofuscinosis, neuronal 10 - loss of speech
- Ceroid lipofuscinosis, neuronal 8 - speech impairment
- Childhood-onset cerebral X-linked adrenoleukodystrophy - speech problems
- Childhood-Onset Schizophrenia - impaired speech
- Choreoathetosis-spasticity, episodic - dysarthria
- Chromosome 10p deletion syndrome - aphonia
- Chromosome 12p duplication syndrome - speech retardation
- Chromosome 12p tetrasomy syndrome - speech retardation
- Chromosome 13 ring syndrome - speech retardation
- Chromosome 15 inverted duplication - speech retardation
- Chromosome 15 Ring - speech retardation
- Chromosome 15q triplication syndrome - speech retardation
- Chromosome 17p, partial deletion - speech retardation
- Chromosome 18 Ring - speech retardation
- Chromosome 18q, partial deletion - speech retardation
- Chromosome 1q duplication syndrome - speech retardation
- Chromosome 2, monosomy 2p22 - speech defect
- Chromosome 20 ring - speech retardation
- Chromosome 22q deletion syndrome - speech retardation
- Chromosome 22q13 deletion - speech difficulties
- Chromosome 22q13.3 deletion syndrome - absent speech
- Chromosome 2p deletion syndrome - speech retardation
- Chromosome 3, trisomy 3p - speech retardation
- Chromosome 4 ring syndrome - speech retardation
- Chromosome 6p deletion syndrome - speech retardation
- Chromosome 7p deletion syndrome - speech retardation
- Chromosome 7p duplication syndrome - speech retardation
- Chromosome 8 trisomy syndrome - speech retardation
- Chromosome 8p mosaic tetrasomy - speech retardation
- Chromosome 8q deletion syndrome - speech retardation
- Chromosome 9q duplication syndrome - speech retardation
- Chromosome partial trisomy 22q11q13 - absence of speech
- Classic childhood ALD - dysarthria (poorly articulated speech)
- Classic migraine - speech difficulty
- Cleft palate - speech defects
- Combarros Calleja Leno syndrome - slow speech
- Congenital Disorders of Glycosylation - dysarthria
- Continuous spike-wave during slow sleep syndrome - aphasia
- Conversion Disorder - aphonia
- Cornelia de Lange Syndrome - abnormal speech development
- Corticobasal Degeneration - hesitant and halting speech
- Creatine deficiency, X-linked - speech delay
- Cri-du-chat syndrome - communication difficulties
- Cyclosporine toxicity - slurred speech
- Déjerine-Roussy syndrome - speaking difficulty
- Davenport-Donlan syndrome - speech defect
- Davis-Lafer syndrome - speech problems
- De Sanctis-Cacchione syndrome - abnormal speech
- Deafness - lymphoedema - leukemia - mutism
- Delayed speech - facial asymmetry - strabismus - ear lobe creases - delayed speech development
- Delirium - incoherent speech
- Demyelinating disorder - Dysarthria
- Developmental dysphasia, familial - speech defect
- Diabetic hypoglycemia - slurred speech
- Dialysis encephalopathy syndrome - dysarthria
- DiGeorge syndrome - speech problems
- Dinno-Shearer-Weisskopf syndrome - speech defect
- Dykes-Markes-Harper syndrome - dysarthria
- Dysphasic dementia, hereditary - speech problems
- Dysphonia, chronic spasmodic - aphonia
- Dystonia 12 - dysarthria
- Dystonia musculorum deforms 4 - speech problems
- Dystonia with cerebellar atrophy - dysarthria
- Dystonias - speech difficulties
- Ectodermal dysplasia - alopecia - preaxial polydactyly - speech defect
- Ectodermal dysplasia - blindness - speech problems
- Ectodermal dysplasia, anhidrotic with T-cell immunodeficiency, autosomal dominant - speech delay
- End Stage Liver Failure - incoherent speech
- Ependymoma - speech problems
- Epilepsy with myoclonic-astatic crisis - slow speech
- Epilepsy, progressive myoclonic 3 - dysarthria
- Episodic ataxia syndrome - slurred speech
- Episodic ataxia, type 1 - slurred speech
- Episodic ataxia, type 2 - dysarthria
- Episodic ataxia, type 5 - dysarthria
- Episodic ataxia, type 6 - slurred speech
- Erythrokeratodermia ataxia - speaking difficulty
- Erythrokeratodermia with ataxia - dysarthria
- FACWA syndrome - dysarthria
- Familial hypertryptophanemia - speech problems
- Familial isolated deficiency of vitamin E - slurred speech
- Familial porencephaly - speech problems
- Fatal familial insomnia - speaking difficulty
- Fazio-Londe syndrome - speaking difficulty
- Fetal alcohol syndrome - speech impairment
- Fitzsimmons-Guilbert syndrome - dysarthria
- Fitzsimmons-Walson-Mellor syndrome - speech defect
- Floating Harbor Syndrome - speech delay
- Foix-Chavany-Marie syndrome - speech difficulty
- FOSMN syndrome - dysarthria
- Freeman-Sheldon Syndrome - speech difficulty
- Fried syndrome - speech defect
- Friedreich ataxia - congenital glaucoma - slow speech
- Friedreich's ataxia - speech problems
- Frontotemporal dementia - altered speech output
- Frostbite - slurred speech
- Fungal meningitis - difficulty talking
- Galactosemia I - speech problems
- Ganglioglioma - speech problems
- Gangliosidosis GM1 type 3 - dysarthria
- German syndrome - speech disorders
- Gerstmann's Syndrome - aphasia
- Ghosal syndrome - speech defect
- Glioblastoma - impaired speech
- Glioma - speech problems
- Gliomatosis cerebri - speech problems
- Gliosarcoma - speech problems
- Glue ear - speech problems
- Glutamate decarboxylase deficiency - speech defect
- Gluten ataxia - dysarthria
- Grand-Kaine-Fulling syndrome - speech problems
- Granulomatous Angiitis of the Central Nervous System - aphasia
- Growth delay - mental retardation - mandibulofacial dysostosis - microcephaly - cleft palate - speech delay
- Heavy metal poisoning - Speech difficulties
- Heidenhain syndrome - dysarthria
- Hemiplegic migraine, familial type 2 - aphasia
- Hemoglobin S/hemoglobin Lepore, Boston - aphasia
- Hemoglobin S/hemoglobin O, Arab - aphasia
- Hemoglobin SC - aphasia
- Hereditary ataxia - speech problems
- Hereditary sensory and autonomic neuropathy 3 - speech problems
- Hereditary Spastic Paraplegia - speaking difficulty
- HERNS syndrome - dysarthria
- Histidinemia - speech retardation
- Homocystinuria - delayed speech development
- Homocystinuria syndrome - delayed speech development
- Howard-Young syndrome - speech defect
- Hunter-MacDonald syndrome - speech problems
- Hydroxyacyl-coa dehydrogenase, type 2, deficiency - dysarthria
- Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome - speech delay
- Hypoglycemia - slurred speech
- Hypoglycemic attack - slurred speech
- Hypomagnesemia primary - dysarthria
- Hypomyelination - congenital cataract - dysarthria
- Hypomyelination - hypogonadotropic hypogonadism - hypodontia - dysarthria
- Hypomyelination and congenital cataract - dysarthria
- Hypothyroidism - slow speech
- Hysteria - loss of speech
- Ichthyosis - alopecia - eclabion - ectropion - mental retardation - speech defect
- Idiopathic facial palsy - difficulty speaking
- Idiopathic hypereosinophilic syndrome - slurred speech
- Impairment of oral perception - speech delay
- Inborn amino acid metabolism disorder - speech problems
- Infantile onset spinocerebellar ataxia - speaking difficulty
- Infantile sialic acid storage disorder - impaired speech
- Intestinal pseudo-obstruction - speech disturbances
- Isoniazid toxicity - slurred speech
- Jankovic-Rivera syndrome - speech defect
- Juvenile pilocytic astrocytoma - speech problems
- Juvenile primary lateral sclerosis - slurred speech
- Katayama fever - aphasia
- Kleine-Levin Syndrome - incoherent speech
- Kocher-Debre-Semelaigne syndrome - speaking difficulty
- Kuru syndrome - aphonia
- Lafora disease - speaking difficulty
- Lhermitte-Cornil-Quesnel syndrome - aphonia
- Lhermitte-McAlpine syndrome - dysarthria
- Lindstrom syndrome - speech defect
- Lissauer paralysis - aphasia
- Locked-in Syndrome - inability to speak
- Low birth weight - dwarfism - dysgammaglobulinemia - speech defect
- Luteinizing hormone releasing hormone, deficiency of, with ataxia - speech defect
- Lymphoedema - atrial septal defects - facial changes - speech delay
- Möbius syndrome - speech difficulties
- Macroglossia - speech problems
- Macrogyria, pseudobulbar palsy and mental retardation - speech defect
- Marchiafava-Bignami disease - speaking difficulty
- Marie type ataxia - speech difficulty
- Marinesco-Sjögren I - speaking difficulty
- Marinesco-Sjogren syndrome - dysarthria
- Marinesco-Sjogren-like syndrome (MSLS) - speech difficulty
- MASA Syndrome - aphasia
- Medulloblastoma - impaired speech
- Meinecke syndrome - speech defect
- Melanoma - astrocytoma syndrome - speech problems
- Mende syndrome - mutism
- Meningioma - aphasia
- Mental retardation - arachnodactyly - hypotonia - telangiectasia - speech defect
- Mental retardation - blepharophimosis - obesity - web neck - speech defect
- Mental retardation - coloboma - slimness - speech defect
- Mental retardation - hip luxation - G6PD variant - speech defect
- Mental retardation - hypotonic facies syndrome, X-linked, 1 - speech defect
- Mental retardation - short broad thumbs - speech defect
- Mental retardation X-linked dysmorphism - speech defect
- Mental retardation X-linked, South African type - mutism
- Mental retardation, Buenos Aires type - speech defect
- Mental retardation, Smith-Fineman-Myers type - speech defect
- Mental retardation, X-linked - acromegaly - hyperactivity - dysarthria
- Mental retardation, X-linked - choreoathesis - abnormal behavior - speech impairment
- Mental retardation, X-linked - dystonia - dysarthria - dysarthria
- Mental retardation, X-linked - gynecomastia - obesity - speech problems
- Mental retardation, X-linked syndromic 12 - aphasia
- Mental retardation, X-linked with brachydactyly and macroglossia - speech problems
- Mental retardation, X-linked, 12 - absent speech
- Mental retardation, X-linked, 16 - speech abnormalities
- Mental retardation, X-linked, 17 - speech problems
- Mental retardation, X-linked, Cabezas type - speech impairment
- Mental retardation, X-linked, syndromic, due to JARID1C mutation - impaired speech
- Mental retardation, X-linked, Vitale type - speech defect
- Mental retardation, X-linked, Wittwer type - speech defect
- Mental retardation, X-linked, Zorick type - inability to speak
- Metachromatic Leukodystrophy - speech abnormalities
- Methylmalonicacidemia with homocystinuria, cbl D - speech problems
- Microcephaly - cervical spine fusion anomalies - speech defect
- Microcephaly - deafness syndrome - speech defect
- Microcephaly, primary autosomal recessive - delayed speech development
- Microcephaly, primary autosomal recessive, 1 - delayed speech development
- Microcephaly, primary autosomal recessive, 2 - delayed speech development
- Microcephaly, primary autosomal recessive, 3 - delayed speech development
- Microcephaly, primary autosomal recessive, 4 - delayed speech development
- Microcephaly, primary autosomal recessive, 5 - delayed speech development
- Microcephaly, primary autosomal recessive, 6 - delayed speech development
- Microencephaly - delayed speech development
- Microphthalmia, syndromic 7 - speech retardation
- Migraine - speech difficulty
- Minamata disease - impaired speech
- MN1 - aphasia
- Moebius axonal neuropathy - hypogonadism - speech problems
- Moebius sequence - speech problems
- MoyaMoya disease 1 - speech disturbances
- MoyaMoya disease 2 - speech disturbances
- MoyaMoya disease 3 - speech disturbances
- Moyamoya Syndrome - speech disturbances
- Multiple system atrophy - slurred speech
- Muscle phosphoglycerate kinase deficiency - aphasia
- Muscular dystrophy, Duchenne and Becker type - dysarthria
- Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency - dysarthria
- Myelinopathies - impaired speech
- Myoclonus - difficulty talking
- Myoclonus hereditary - progressive distal muscular atrophy - speech defect
- Myoclonus, cerebellar ataxia, deafness - speech problems
- Myopathy and diabetes mellitus - dysarthria
- Myxedema - slow speech
- Nasopharyngeal carcinoma - difficulty speaking
- Neuroaxonal dystrophy - renal tubular acidosis - speech defect
- Neurofibromatosis syndrome - speech disorders
- Neurofibromatosis syndrome Type II - speech disorders
- Neurofibromatosis-2 - speech difficulty
- Neuroleptic Malignant Syndrome - speaking difficulty
- Neuronal intranuclear inclusion disease - speech defect
- Neurosarcoidosis - impaired speech
- Neurosyphilis - dysarthria
- Nielsen-Jacobs syndrome - inability to speak
- Non-lissencephalic cortical dysplasia - speech delay
- Oculodentoosseous dysplasia dominant - dysarthria
- Olivopontocerebellar Atrophy - slurred speech (dysarthria)
- Olivopontocerebellar atrophy I - speech disturbances
- Olivopontocerebellar atrophy type IV - speech difficulties
- Opsoclonus Myoclonus - dysphasia (difficulty speaking)
- Optic atrophy 2 - dysarthria
- Oral submucous fibrosis - impaired speech
- Oral-facial cleft - speech problems
- Orofaciodigital syndrome type1 - dysarthria
- Oromandibular-limb hypogenesis spectrum - speech difficulties
- Oto-Palatal-digital syndrome - speech retardation
- Oto-Palato-digital syndrome type 1 - speech retardation
- Pallidopyramidal syndrome - dysarthria
- Pantothenate kinase-associated neurodegeneration - speaking difficulty
- Paraneoplastic cerebellar degeneration - dysarthria
- Parenchymatous cortical degeneration of cerebellum - slurred speech
- Parkinson disease 3 - speech problems
- Parkinson disease 9 - speech problems
- Partington-Anderson syndrome - speech defect
- Passos-Bueno syndrome - absent speech
- Pellagra-like syndrome - dysarthria
- Pena Shokeir syndrome, type 1 - speech problems
- Perisylvian syndrome - speaking difficulty
- Phenytoin toxicity - slurred speech
- Phosphoribosylpyrophosphate synthetase superactivity - speech defect
- Pick's Disease - speech disturbances
- Pick's disease of the brain - altered sppech output
- Podder-Tolmie syndrome - speech defect
- Poikilodermatomyositis - mental retardation - speech defect
- Polychondritis - speech difficulties
- Primary angiitis of the central nervous system - aphasia
- Prion diseases - inability to speak
- Progressive Multifocal Leukoencephalopathy - speech disturbances
- Progressive Spinobulbar muscular atrophy - dysarthria (speech impairment)
- Progressive supranuclear palsy, atypical - dysarthria
- Pseudoadrenoleukodystrophy - speech defect
- Pseudoobstruction idiopathic intestinal - speech disturbances
- Pseudopapilledema - blepharophimosis - hand anomalies - speech defect
- Pseudoprogeria syndrome - speech defect
- Quinsy - difficulty talking
- Radiation induced meningioma - aphasia
- Radioulnar synostosis mental retardation hypotonia - speech defect
- Rajab-Spranger syndrome - speech defect
- Ramsay Hunt II - speaking difficulty
- Rapp-Hodgkin syndrome - speech difficulties
- Rasmussen subacute encephalitis - aphasia
- Riedel syndrome - aphonia
- Roy-Maroteaux-Kremp syndrome - speech defect
- Rubinstein-Taybi Syndrome - speech difficulties
- Sanfilippo syndrome type A - delayed speech development
- Sanfilippo syndrome type B - delayed speech development
- Say-Barber-Miller syndrome - speech defect
- Say-Carpenter syndrome - speech defect
- Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis - dysarthria
- Short stature mental retardation eye anomalies - speech defect
- Shy-Drager Syndrome - speech difficulties
- Sialuria, Finnish type - dysarthria
- Simpson-Golabi-Behmel syndrome, type 1 (SGBS1) - speech problems
- Sinus cancer - Speech changes
- Smith-Fineman-Myers syndrome 2 - speech defect
- Spastic ataxia, Charlevoix-Saguenay type - dysarthria
- Spastic dysphonia - speaking difficulty
- Spastic paraplegia 11, autosomal recessive - dysarthria
- Spastic paraplegia 15, autosomal recessive - dysarthria
- Spastic paraplegia 2, X-linked - dysarthria
- Spastic paraplegia 20, autosomal recessive - dysarthria
- Spastic paraplegia 7, autosomal recessive - dysarthria
- Spastic paraplegia glaucoma precocious puberty - speech defect
- Spastic paraplegia type 5A, recessive - dysarthria
- Spastic paraplegia with precocious puberty - dysarthria
- Spinal bulbar motor neuropathy - slurred speech
- Spinocerebellar Ataxia - Speech impairment
- Spinocerebellar ataxia - dysmorphism - dysarthria
- Spinocerebellar ataxia 10 - dysarthria
- Spinocerebellar ataxia 11 - dysarthria
- Spinocerebellar ataxia 12 - dysarthria
- Spinocerebellar ataxia 13 - dysarthria
- Spinocerebellar ataxia 14 - dysarthria
- Spinocerebellar ataxia 15 - dysarthria
- Spinocerebellar ataxia 16 - dysarthria
- Spinocerebellar ataxia 17 - dysarthria
- Spinocerebellar ataxia 18 - dysarthria
- Spinocerebellar ataxia 20 - speech problems
- Spinocerebellar ataxia 21 - speech problems
- Spinocerebellar ataxia 22 - dysarthria
- Spinocerebellar ataxia 23 - speech problems
- Spinocerebellar ataxia 26 - dysarthria
- Spinocerebellar ataxia 27 - dysarthria
- Spinocerebellar ataxia 28 - dysarthria
- Spinocerebellar ataxia 29 - dysarthria
- Spinocerebellar ataxia 3 - dysarthria
- Spinocerebellar ataxia 4 - speaking difficulty
- Spinocerebellar ataxia 5 - speaking difficulty
- Spinocerebellar ataxia 8 - slow speech
- Spinocerebellar ataxia, autosomal dominant - speech defect
- Spinocerebellar ataxia, autosomal recessive 1 - dysarthria
- Spinocerebellar ataxia, autosomal recessive 2 - dysarthria
- Spinocerebellar ataxia, autosomal recessive 4 - dysarthria
- Spinocerebellar ataxia, autosomal recessive 6 - delayed speech development
- Spinocerebellar ataxia, autosomal recessive 7 - dysarthria
- Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy - dysarthria
- Spinocerebellar ataxia, Machado-Joseph type I - dysarthria
- Spinocerebellar ataxia, Machado-Joseph type II - dysarthria
- Spinocerebellar ataxia, Machado-Joseph type III - dysarthria
- Spinocerebellar ataxia, Machado-Joseph type IV - dysarthria
- Spinocerebellar ataxia, Machado-Joseph type V - dysarthria
- Spinocerebellar ataxia, X-linked, 5 - dysarthria
- Spinocerebellar ataxia-dysmorphism syndrome - speaking difficulty
- Spinocerebellar degenerescence, book type - speech defect
- Spondyloepimetaphyseal dysplasia, X linked with mental deterioration - dysarthria
- Spondylometaphyseal dysplasia, X-linked - speech impairment
- Spongiform encephalopathy - speaking difficulty
- SSADH deficiency (succinic semialdehyde dehydrogenase deficiency) - delayed speech development
- Stroke - speech problems
- Subarachnoid hemorrhage - speech problems
- Sydenham chorea - speaking difficulty
- Syringobulbia - speaking difficulty
- Takayasu arteritis - aphasia
- Thanatophoric dysplasia, type 1 - speech retardation
- Thanatophoric dysplasia, type 2 - speech retardation
- Thiele syndrome - speech defect
- Thrombocytopathy - asplenia - miosis - speech defect
- Thumb deformity, alopecia, pigmentation anomaly - speech defect
- Thyroid cancer - difficulty speaking
- Todd's Paralysis - speech problems
- Tome-Brune-Fardeau syndrome - speech defect
- Torsion dystonia - speech difficulty
- Torsion dystonia, autosomal dominant - speech difficulty
- Torsion dystonia, autosomal recessive - speech difficulty
- Torsion dystonia, X-linked - speech difficulty
- Tranebjaerg-Svejgaard syndrome - speech defect
- Transient Ischemic Attack - difficulty talking
- Treft-Sanborn-Carey syndrome - speech defect
- Tremor hereditary essential, 1 - dysarthria
- Tremor hereditary essential, 2 - dysarthria
- Trigonocephaly - ptosis - mental retardation - speech defect
- Trihydroxycholestanoylcoa oxidase isolated deficiency - dysarthria
- Trisomy 8 mosaicism - speech delay
- Tropical Spastic Paraparesis - speaking difficulty
- Vacinko syndrome - mutism
- Variant CJD - loss of speech
- Vascular malformations of the brain - impaired speech
- Vogt-Koyanagi-Harada Syndrome - aphasia
- W syndrome - Speech problems
- Water Intoxication - slurred speech
- Weaver Syndrome - slurred speech
- West African Trypanosomiasis - difficulty talking
- Western/Eastern/California encephalitis - Aphasia
- Westphal-Leyden ataxia - speech problems
- Wiedemann-Tolksdorf syndrome - delayed speech development
- Wilson's Disease - Dysarthria
- Wittwer sydnrome - Absence of speech
- Wolfram's disease - Dysarthria
- Wyburn Mason's syndrome - aphasia
- X fragile site folic acid type - Speech delay
- X-linked hydrocephalus spectrum - aphasia
- X-linked mental retardation craniofacial abnormal microcepahly club - Speech difficulties
- Xeroderma pigmentosum - abnormal speech
- Xeroderma pigmentosum, type 1 - delayed speech development
- Xeroderma pigmentosum, type 2 - delayed speech development
- Xeroderma pigmentosum, type 4 - abnormal speech
- Xeroderma pigmentosum, type 7 - abnormal speech
All Causes of Speech symptoms
The full list of all possible causes for Speech symptoms described in various sources is as follows:
- 1q deletion - speech retardation
- 3-methylglutaconic aciduria, type 1 - speech delay
- 3C syndrome - speech defect
- 3q deletion - speech retardation
- Aarskog-Ose-Pande syndrome - delayed speech development
See full list of possible disease causes of Speech symptoms
Drug side effect causes of Speech symptoms
The following drugs, medications, substances or toxins may possibly cause Speech symptoms as a side effect.- Topiramate
- Topamax
- Topamax Sprinkle
- Neurontin
- Tiagabine
Drug interaction causes of Speech symptoms:
Drug interactions may be a possible cause of Speech symptoms.- Primidone and Isocarboxazid interaction
- Apo-Primidone and Isocarboxazid interaction
- Myidone and Isocarboxazid interaction
- Mysoline and Isocarboxazid interaction
- PMS-Primidone and Isocarboxazid interaction
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