Schizencephaly

Orpha code: 799OMIM code: 269160

Definition

A rare developmental defect during embryogenesis characterized by the presence of linear clefts containing cerebrospinal fluid lined by abnormal grey matter that extend from the lateral ventricles to the pial surface of the cortex. Schizencephaly can involve one or both cerebral hemispheres and may lead to a variety of neurological symptoms such as epilepsy, motor deficits, and psychomotor retardation.

Disease data
Classification

Disease

ORPHA code
799
OMIM code
269160
ICD10 code
Q04.6
ICD11 code
LA05.61

No additional description.

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