Lissencephaly with cerebellar hypoplasia type A
ORPHA:100011· ICD-10 Q04.3
Definition
A rare, genetic, lissencephaly with cerebellar hypoplasia subtype characterized by classical lissencephaly with thickened cortical gray matter (with either no discernable gradient, a predominantly posterior gradient, or a predominantly anterior gradient) associated with variable, predominantly midline, cerebellar hypoplasia.
- Age of onset
- Antenatal, Neonatal