Lissencephaly type 1 due to doublecortin gene mutation
Lissencephaly type 1 due to doublecortin gene mutation
Definition
Type 1 lissencephaly due to doublecortin (DCX) gene mutations is a semi-dominant X-linked disease characterized by intellectual deficiency and seizures that are more severe in male patients.
Also known as lissencephaly type 1 due to doublecortin gene mutation, lissencephaly, X-linked, lissencephaly, X-linked, type 1, subcortical laminal heterotopia, X-linked, X-linked lissencephaly type 1 — per MONDO