Lissencephaly due to LIS1 mutation

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Name:
Lissencephaly due to LIS1 mutation
Description:
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.
ORPHAcode:
95232
Synonyms:
PAFAH1B1-related lissencephaly
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14