Causes of Hydrocephalus
List of causes of Hydrocephalus
Following is a list of causes or underlying conditions
(see also Misdiagnosis of underlying causes of Hydrocephalus)
that could possibly cause Hydrocephalus includes:
- Congenital defects
- Meningitis
- Head injury
- Brain hemorrhage (see Brain symptoms)
- Brain tumor
- Cerebral Aneurysm - hydrocephalus
- Osteopetrosis, autosomal recessive 2 - hydrocephalus
- Osteogenesis imperfecta, type 2 - hydrocephalus
- Meningoencephalocele - hydrocephalus
- Malignant germ cell tumor - hydrocephalus
- Intermediate cystinosis - hydrocephalus
- Glycine synthase deficiency, type 1 - hydrocephalus
- Czeizel-Losonci syndrome - hydrocephalus
- Czeizel syndrome - hydrocephalus
- Toxoplasma, congenital
- X-linked hydrocephalus spectrum - hydrocephalus
- Warfarin syndrome - Hydrocephalus
- Sjögren-Larsson syndrome - hydrocephalus
- Glycine synthase deficiency, type 2 - hydrocephalus
- Dandy-Walker - facial hemangioma - hydrocephalus
- Cardiofaciocutaneous Syndrome - hydrocephalus
- Walker-Warburg syndrome - hydrocephalus
- I-cell disease
- Arnold-Chiari malformation
- Spina bifida - hydrocephalus
- Smith-Lemli-Opitz syndrome, type 2 - hydrocephalus
- Schizencephaly - hydrocephalus
- Rokitansky Van Bogaert syndrome - hydrocephalus
- Mental retardation, Buenos Aires type - hydrocephalus
- Gliomatosis cerebri - hydrocephalus
- Endodermal sinus tumor - hydrocephalus
- Chromosome 7q duplication syndrome - hydrocephalus
- Chromosome 6p deletion syndrome - hydrocephalus
- Chromosome 12q duplication syndrome - hydrocephalus
- Axial mesodermal dysplasia spectrum - hydrocephalus
- Subarachnoid haemorrhage
- Arachnoid cyst
- Aneurysm, intracranial berry, 1 - hydrocephalus
- Triploid syndrome - hydrocephalus
- Silverman-Handmaker syndrome - hydrocephalus
- Renal-hepatic-pancreatic dysplasia - Dandy Walker cyst - hydrocephalus
- Porencephaly - hydrocephalus
- Pineoblastoma, adult - hydrocephalus
- Mucopolysaccharidosis type 2 Hunter syndrome- severe form - hydrocephalus
- Meningomyelocele - hydrocephalus
- Meningocele - hydrocephalus
- Krause syndrome - hydrocephalus
- Chromosome 22q duplication syndrome - hydrocephalus
- Cennamo-Gangemi syndrome - hydrocephalus
- Bone marrow failure - neurologic abnormalities - hydrocephalus
- Bobble-head doll syndrome - hydrocephalus
- Biemond syndrome type 2 - hydrocephalus
- Alexander Syndrome - hydrocephalus
- Guillain-Barre syndrome
- Intraventricular haemorrhage
- Sulfatidosis juvenile, Austin type - hydrocephalus
- Subarachnoid hemorrhage - hydrocephalus
- Aneurysm, intracranial berry, 2 - hydrocephalus
- Vein of Galen aneurysm - Hydrocephalus
- Rolland-Desbuquois syndrome - hydrocephalus
- Rhombencephalosynapsis - hydrocephalus
- Pinealoma - hydrocephalus
- Neonatal bacterial meningitis - hydrocephalus
- Infantile sialic acid storage disorder - hydrocephalus
- Hydranencephaly - hydrocephalus
- Ependymoma - hydrocephalus
- Encephaloceles - hydrocephalus
- Coffin-Lowry syndrome - hydrocephalus
- CMV antenatal infection - hydrocephalus
- Chromosome 8p deletion syndrome - hydrocephalus
- BRESHECK syndrome
- Mucosulfatidosis
- Normal pressure hydrocephalus
- Aneurysm, intracranial berry, 3 - hydrocephalus
- Thanatophoric dysplasia, type 1 - hydrocephalus
- Osteogenesis imperfecta, type IIB - hydrocephalus
- Intracranial germ cell tumour - hydrocephalus
- Dandy-Walker malformation postaxial polydactyly - hydrocephalus
- Craniofacial conodysplasia - hydrocephalus
- Cerebral ventricle neoplasm - hydrocephalus
- Acutane embryopathy - hydrocephalus
- Aneurysm, intracranial berry, 4 - hydrocephalus
- Waaler Aarskog syndrome - hydrocephalus
- Thanatophoric dysplasia, type 2 - hydrocephalus
- Optic pathway glioma - hydrocephalus
- Marie-Seé Syndrome - hydrocephalus
- Hydrocephalus - growth retardation - skeletal anomalies - hydrocephalus
- Hajdu-Cheney Syndrome - hydrocephalus
- Fried syndrome - hydrocephalus
- Deletion 2q24 - hydrocephalus
- Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus - hydrocephalus
- Arnold-Chiari malformation type 2 - hydrocephalus
- Microphthalmia-dermal aplasia-sclerocornea syndrome
- Scheie disease
- Alpha-L-iduronidase deficiency
- Basilar impression primary - hydrocephalus
- Aneurysm, intracranial berry, 5 - hydrocephalus
- Transthyretin amyloidosis - hydrocephalus
- Sengers-Hamel-Otten syndrome - hydrocephalus
- Kleeblattschaedel syndrome - hydrocephalus
- Glycine synthase deficiency - hydrocephalus
- Chromosome 1q duplication syndrome - hydrocephalus
- Campomelic dysplasia - hydrocephalus
- Arnold-Chiari malformation type 3 - hydrocephalus
- Aneurysm, intracranial berry, 6 - hydrocephalus
- Partial agenesis of corpus callosum - hydrocephalus
- Neurosyphilis - hydrocephalus
- Midline field defects - hydrocephalus
- Larsen syndrome, recessive type - hydrocephalus
- Jeune syndrome - hydrocephalus
- Isotretinoin embryopathy like syndrome - hydrocephalus
- Hydrocephalus due to congenital stenosis of aqueduct of sylvius - hydrocephalus
- Congenital Toxoplasmosis - hydrocephalus
- Chromosome 16q, partial deletion - hydrocephalus
- Beemer-Ertbruggen syndrome - hydrocephalus
- Corpus callosum agenesis type 2
- Muscle-eye-brain disease
- Osteopetrosis lethal - hydrocephalus
- Aneurysm, intracranial berry, 7 - hydrocephalus
- Aneurysm, intracranial berry - hydrocephalus
- Schwartz, Cohen-Addad, Lambert syndrome - hydrocephalus
- Pineal Teratoma - hydrocephalus
- Osteogenesis imperfecta, type 2A - hydrocephalus
- Macrocephaly, mental retardation, short stature, spastic paraplegia and CNS malformations - hydrocephalus
- HARD syndrome - hydrocephalus
- Encephalocele frontal - hydrocephalus
- Encephalocele anterior - hydrocephalus
- Chromosome 4, Monosomy 4q - hydrocephalus
- Chromosome 14 uniparental disomy syndrome - hydrocephalus
- Cat Eye Syndrome - hydrocephalus
- BOR-Duane hydrocephalus contiguous gene syndrome - hydrocephalus
- Hydrocephalus, X-linked
- Dandy-Walker syndrome - Hydrocephalus
- Cloverleaf skull syndrome
- Neural tube defects
- Aneurysm, intracranial berry, 8 - hydrocephalus
- VACTERYL hydrocephaly - Hydrocephalus
- VACTERL association with hydrocephaly, X-linked - Hydrocephalus
- Seow-Najjar syndrome - hydrocephalus
- Sabin-Feldman syndrome - hydrocephalus
- Rhabdoid tumor - hydrocephalus
- Pseudoaminopterin syndrome - hydrocephalus
- Pfeiffer syndrome Type 3 - hydrocephalus
- Neurocutaneous melanosis - hydrocephalus
- Nephropathic cystinosis - hydrocephalus
- Microphthalmia, syndromic 7 - hydrocephalus
- Megalencephaly - polymicrogyria - post-axial polydactyly - hydrocephalus - hydrocephalus
- Faye-Petersen-Ward-Carey syndrome - hydrocephalus
- Corpus callosum, agenesis of, blepharophimosis Robin type - hydrocephalus
- Chromosome 5p duplication syndrome - hydrocephalus
- Baker-Vinters syndrome - hydrocephalus
- Neurocysticercosis - hydrocephalus
- Alveolar hydatid disease
- Aqueduct stenosis
- Adams-Oliver syndrome
- Alexander disease
More causes:
see full list of causes for Hydrocephalus
Causes of Hydrocephalus (Diseases Database):
The follow list shows some of the possible medical causes of Hydrocephalus
that are listed by the Diseases Database:
Source: Diseases Database
Hydrocephalus Causes: Book Excerpts
Hydrocephalus as a complication of other conditions:
Other conditions that might have
Hydrocephalus as a complication may,
potentially, be an underlying cause of Hydrocephalus.
Our database lists the following as having
Hydrocephalus as a complication of that condition:
- 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
- Basilar impression primary
- Cerebral Aneurysm
- Meningitis
- Meningococcal A
- Meningococcal C
- Meningococcal disease
- Osteopetrosis lethal
- Pfeiffer Syndrome Type I
- Pneumococcal meningitis
- Spina bifida
- Subarachnoid hemorrhage
- Sulfatidosis juvenile, Austin type
Hydrocephalus as a symptom:
Conditions listing Hydrocephalus
as a symptom may also be potential underlying causes of Hydrocephalus.
Our database lists the following as having
Hydrocephalus as a symptom of that condition:
- Accutane - Teratogenic Agent
- Acrocephalopolydactyly
- Acrocephalosyndactyly Syndrome type 5
- Acrocephalosyndactyly type 5 (ACPS 5)
- Acutane embryopathy
- Acyclovir - Teratogenic Agent
- Alexander Syndrome
- Aminopterin and methotrexate - Teratogenic Agent
- Arnold-Chiari malformation type 2
- Arnold-Chiari malformation type 3
- Autosomal Recessive Tetra-Amelia
- Axial mesodermal dysplasia spectrum
- Baker-Vinters syndrome
- Beemer-Ertbruggen syndrome
- Biemond syndrome type 2
- Bobble-head doll syndrome
- Bone marrow failure - neurologic abnormalities
- BOR-Duane hydrocephalus contiguous gene syndrome
- Braddock Jones Superneau syndrome
- Brain cancer
- Campomelic dwarfism
- Campomelic dysplasia
- Cardiofaciocutaneous Syndrome
- Cat Eye Syndrome
- Cennamo-Gangemi syndrome
- Cerebral ventricle neoplasm
- Chromosome 1, 1p36 deletion syndrome
- Chromosome 12, trisomy 12q
- Chromosome 12q duplication syndrome
- Chromosome 14 uniparental disomy syndrome
- Chromosome 16q, partial deletion
- Chromosome 1q duplication syndrome
- Chromosome 2, monosomy 2q24
- Chromosome 22q duplication syndrome
- Chromosome 4, Monosomy 4q
- Chromosome 5, Trisomy 5p
- Chromosome 5p duplication syndrome
- Chromosome 6, trisomy 6p
- Chromosome 6p deletion syndrome
- Chromosome 7, trisomy 7q
- Chromosome 7q duplication syndrome
- Chromosome 8, monosomy 8q
- Chromosome 8p deletion syndrome
- Cloverleaf skull micromelia thoracic dysplasia
- CMV antenatal infection
- Coffin-Lowry syndrome
- Congenital Toxoplasmosis
- Corpus callosum agenesis - blepharophimosis - Robin sequence
- Corpus callosum, agenesis of, blepharophimosis Robin type
- Craniofacial conodysplasia
- Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus
- Czeizel syndrome
- Czeizel-Losonci syndrome
- Dandy-Walker - facial hemangioma
- Dandy-Walker malformation postaxial polydactyly
- Dandy-Walker Syndrome
- Del(1) (23-q25)
- Del(1) (q24-q25.3)
- Del(1) (q41-qter)
- Del(1q32)
- Deletion 2q24
- Deletion 8q
- Dup (1) (q23-qter) and del (3)(pter-p25)
- Dup (1) (q32-qter) and del (7)(q32-qter)
- Duplication 12q
- Duplication 5p
- Duplication 6p
- Duplication 7q
- Emanuel syndrome
- Encephalocele anterior
- Encephalocele frontal
- Encephaloceles
- Endodermal sinus tumor
- Ependymoma
- Ergotamine - Teratogenic Agent
- Faye-Petersen-Ward-Carey syndrome
- Fried syndrome
- Gliomatosis cerebri
- Glycine synthase deficiency
- Glycine synthase deficiency, type 1
- Glycine synthase deficiency, type 2
- Hajdu-Cheney Syndrome
- HARD syndrome
- HARD syndrome (Hydrocephalus - agyria - retinal dysplasia)
- Hydranencephaly
- Hydrocephalus - craniosynostosis - bifid nose
- Hydrocephalus - growth delay - skeletal anomalies
- Hydrocephalus - growth retardation - skeletal anomalies
- Hydrocephalus - Skeletal Anomalies - Mental Disturbance
- Hydrocephalus due to congenital stenosis of aqueduct of sylvius
- Hydrocephalus obesity hypogonadism
- Hydrocephalus skeletal anomalies
- Hypothalamic hamartomas
- Infantile sialic acid storage disorder
- Iniencephaly
- Intermediate cystinosis
- Intracranial germ cell tumour
- Isotretinoin - Teratogenic Agent
- Isotretinoin embryopathy like syndrome
- Jeune syndrome
- Kleeblattschaedel syndrome
- Krause syndrome
- Larsen syndrome, recessive type
- Macrocephaly, mental retardation, short stature, spastic paraplegia and CNS malformations
- Malignant germ cell tumor
- Malignant rhabdoid tumors
- Marie-Seé Syndrome
- Megalencephaly - polymicrogyria - post-axial polydactyly - hydrocephalus
- Meningocele
- Meningoencephalocele
- Meningomyelocele
- Mental retardation, Buenos Aires type
- Micromelic bone dysplasia with cloverleaf skull
- Microphthalmia, syndromic 7
- Midline field defects
- Monosomy 1p36
- Mucopolysaccharidosis type 2 Hunter syndrome- severe form
- Neonatal bacterial meningitis
- Nephropathic cystinosis
- Neurocutaneous melanosis
- Neurocysticercosis
- Neurosyphilis
- Optic pathway glioma
- Osteogenesis imperfecta, type 2
- Osteogenesis imperfecta, type 2A
- Osteogenesis imperfecta, type IIB
- Osteopetrosis, autosomal recessive 2
- Partial agenesis of corpus callosum
- Pfeiffer syndrome Type 3
- Pfeiffer Syndrome Type I
- Pineal Teratoma
- Pinealoma
- Pineoblastoma, adult
- Porencephaly
- Pseudoaminopterin syndrome
- Renal-hepatic-pancreatic dysplasia - Dandy Walker cyst
- Rhabdoid tumor
- Rhombencephalosynapsis
- Rokitansky Van Bogaert syndrome
- Rolland-Desbuquois syndrome
- Sabin-Feldman syndrome
- Schinzel Giedion Syndrome
- Schizencephaly
- Schwartz, Cohen-Addad, Lambert syndrome
- Sengers-Hamel-Otten syndrome
- Seow-Najjar syndrome
- Silverman-Handmaker syndrome
- Sjogren-Larsson syndrome
- Sjögren-Larsson syndrome
- Smith-Lemli-Opitz syndrome, type 2
- Tetra-Amelia, Autosomal Recessive
- Thanatophoric dysplasia, type 1
- Thanatophoric dysplasia, type 2
- Toxoplasmosis - Teratogenic Agent
- Transthyretin amyloidosis
- Triploid syndrome
- VACTERL association with hydrocephaly, X-linked
- VACTERYL hydrocephaly
- Vein of Galen aneurysm
- Waaler Aarskog syndrome
- Walker-Warburg Syndrome
- Warfarin syndrome
- X-linked hydrocephalus spectrum
Related information on causes of Hydrocephalus:
As with all medical conditions,
there may be many causal factors.
Further relevant information on causes of Hydrocephalus may be found in:
Causes of Hydrocephalus: Online Medical Books
16 MEDICAL BOOKS ONLINE!
Review excerpts from medical books online, free, without registration,
for more information about the causes of Hydrocephalus.
Hydrocephalus:
Causes and incidence
(Professional Guide to Diseases (Eighth Edition))
Hydrocephalus may result from an obstruction in CSF flow (noncommunicating hydrocephalus) or from faulty absorption of CSF (communicating hydrocephalus). (See Normal circulation of CSF.)
In noncommunicating hydrocephalus, the obstruction occurs most frequently between the third and fourth ventricles, at the aqueduct of Sylvius, but it can also occur at the outlets of the fourth ventricle (foramina of Luschka and Magendie) or, rarely, at the foramen of Monro. This obstruction may result from faulty fetal development, infection (syphilis, granulomatous diseases, meningitis), a tumor, cerebral aneurysm, or a blood clot (after intracranial hemorrhage).
In communicating hydrocephalus, faulty absorption of CSF may result from surgery to repair a myelomeningocele, adhesions between meninges at the base of the brain, or meningeal hemorrhage. Rarely, a tumor in the choroid plexus causes overproduction of CSF, producing hydrocephalus.
Hydrocephalus occurs most commonly in neonates but can also occur in adults as a result of injury or disease. It affects 1 of every 1,000 people.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Diseases (Eighth Edition), 2005
Hydrocephalus:
Causes
(Handbook of Diseases)
Hydrocephalus may result from an obstruction in CSF flow (noncommunicating hydrocephalus) or from faulty absorption of CSF (communicating hydrocephalus).
Noncommunicating hydrocephalus
In noncommunicating hydrocephalus, the obstruction occurs most commonly between the third and fourth ventricles, at the aqueduct of Sylvius, but it can also occur at the outlets of the fourth ventricle (foramina of Luschka and Magendie) or, rarely, at the foramen of Monro.
This obstruction may result from faulty fetal development, infection (syphilis, granulomatous diseases, meningitis), a tumor, a cerebral aneurysm, or a blood clot (after intracranial hemorrhage).
Communicating hydrocephalus
In communicating hydrocephalus, faulty absorption of CSF may result from surgery to repair a myelomeningocele, adhesions between meninges at the base of the brain, or meningeal hemorrhage. Rarely, a tumor in the choroid plexus causes overproduction of CSF, producing hydrocephalus.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Diseases, 2003
Verbal Communication Difficulty:
Principal Causes of Verbal Communication Difficulty
(The Diagnostic Approach to Symptoms and Signs in Pediatrics)
- Receptiveand expressive language disorders
- Maturational delay
- Hearing loss
- Neurologic disorders
- Psychologic disorders
- Speech disorders
- Articulationdisorders
- Phonology disorders
- Fluency disorders
- Voice disorders
- Phonationdisorders
- Resonance disorders
» READ BOOK EXCERPT ONLINE »
Source: The Diagnostic Approach to Symptoms and Signs in Pediatrics, 2006
Hydrocephalus:
Hydrocephalus - pathophysiology
(The 5-Minute Pediatric Consult)
- Normal pathway of CSF: Choroid plexus and interstitial fluid (sources), lateral ventricles, foramina of Monro, 3rd ventricle, aqueduct of Sylvius, 4th ventricle, foramina of Luschka and Magendie, subarachnoid space, arachnoid villi, and venous circulation
- Hydrocephalus results from obstruction to CSF flow, impaired reabsorption, or overproduction of CSF.
- Noncommunicating (obstructive) hydrocephalus results from obstruction within the ventricular system.
- Communicating hydrocephalus usually results from impaired CSF reabsorption or (rarely) overproduction (e.g., due to a choroid plexus papilloma).
- The noncommunicating/communicating distinction has no prognostic significance, but has implications for etiology and choice of therapeutic intervention.
Hydrocephalus - etiology
- Intraventricular hemorrhage is most commonly due to prematurity, but may also occur with trauma. It results in impaired CSF absorption due to meningeal adhesions, granular ependymitis, and clots. Posthemorrhagic hydrocephalus (PHH) occurs in 35% of all neonates surviving intraventricular hemorrhage; its incidence increases with increasing severity of hemorrhage.
- Tumors or cysts near the foramina or the aqueduct, or within the ventricular system
- Infection (meningitis, intrauterine infection) can lead to leptomeningeal adhesions and granulations which block reabsorption of CSF.
- Developmental:
- Chiari malformation, type II (associated with myelomeningocele, brain migrational disorders, small posterior fossa, inferior displacement of medulla and cerebellar vermis, kinking of the brainstem, aqueductal stenosis, beaking of the tectum)
- Dandy-Walker malformation (absence of cerebellar vermis, small cerebellar hemispheres, enlarged posterior fossa, often with cystic 4th ventricle)
- X-linked and autosomal dominant hydrocephalus; the former is often associated with aqueductal stenosis and mutations in L1CAM on Xq28.
- Sporadic primary aqueductal stenosis
- Dysmorphic syndromes (e.g., Apert syndrome, Cockayne syndrome, Crouzon syndrome, Pfeiffer syndrome, trisomy 13, trisomy 18, trisomy 21, triploidy)
- Alexander disease
- Mucopolysaccharidoses (e.g., type II (Hunter), type VI, (Maroteaux-Lamy)
- Migrational disorders/congenital muscular dystrophies (e.g., Miller-Dieker, muscle-eye-brain disease, Fukuyama congenital muscular dystrophy, Walker-Warburg syndrome)
- Achondroplasia
- Neurocutaneous syndromes (e.g., neurofibromatosis type 1, rare)
- Idiopathic
» READ BOOK EXCERPT ONLINE »
Source: The 5-Minute Pediatric Consult, 2008
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