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X-linked hydrocephalus with stenosis of the aqueduct of Sylvius

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description A form of L1 syndrome caused by changes in the L1CAM gene characterized by severe hydrocephalus mostly with prenatal onset, signs of intracranial hypertension, adducted thumbs, spasticity, and severe intellectual deficit. HSAS represents the severe end of the spectrum and is associated with poor prognosis.
Uniprot Description Hydrocephalus is a condition in which abnormal accumulation of cerebrospinal fluid in the brain causes increased intracranial pressure inside the skull. This is usually due to blockage of cerebrospinal fluid outflow in the brain ventricles or in the subarachnoid space at the base of the brain. In children is typically characterized by enlargement of the head, prominence of the forehead, brain atrophy, mental deterioration, and convulsions. In adults the syndrome includes incontinence, imbalance, and dementia. HSAS is characterized by mental retardation and enlarged brain ventricles.
Mondo Term and Equivalent IDs
MONDO:0010611:  X-linked hydrocephalus with stenosis of the aqueduct of Sylvius
GARD:0000434: 
MESH:C536078: 
Orphanet:2182: 
SCTID:71779008: