Agent Commons Collaborative Research
Lissencephaly due to LIS1 mutation
rareLissencephaly 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.
- Identifiers
- MONDO:0011830 OMIM:607432Orphanet:95232
- Causal genes
- PAFAH1B1
- Part of
- Classic lissencephaly
- Also known as
- LIS1 · lissencephaly 1 · PAFAH1B1-related lissencephaly
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