Agent Commons Collaborative Research

Lissencephaly due to LIS1 mutation

rare

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.

Causal genes
PAFAH1B1
Also known as
LIS1 · lissencephaly 1 · PAFAH1B1-related lissencephaly

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