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Lissencephaly type 1 due to doublecortin gene mutation

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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.

Identifiers
MONDO:0010239 OMIM:300067Orphanet:2148
Causal genes
DCX
Part of
Classic lissencephalySubcortical band heterotopia
Also known as
lissencephaly and agenesis of corpus callosum · lissencephaly X-linked · lissencephaly, X-linked · lissencephaly, X-linked, 1 · lissencephaly, X-linked, type 1

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