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Лісенцефалія внаслідок мутації LIS1

ORPHA:95232· ICD-10 Q04.3· Lissencephaly due to LIS1 mutation

Визначення(English summary)

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.

Успадкування
Autosomal dominant
Вік початку
Antenatal, Infancy, Neonatal