Lissencephaly due to LIS1 mutation

Orpha code: 95232OMIM code: 607432

Definition

Lissencephaly due to LIS1 mutation is a cerebral malformation with epilepsy characterized predominantly by posterior isolated lissencephaly with developmental delay, intellectual disability and epilepsy that usually evolves from West syndrome to Lennox-Gastaut syndrome. Additional features include muscular hypotonia, acquired microcephaly, failure to thrive and poor control of airways leading to aspiration pneumonia.

Disease data
Classification

Disease

Synonyms
PAFAH1B1-related lissencephaly
Lizencefalia związana z PAFAH1B1
ORPHA code
95232
OMIM code
607432
ICD10 code
Q04.3
ICD11 code
-

No additional description.

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