Lissencephaly due to LIS1 mutation

Orpha code: 95232OMIM code: 607432

Definicja

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
Klasyfikacja

Disease

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

No additional description.

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