Lissencephaly type 1 due to doublecortin gene mutation

MONDO:0010239

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: X-linked lissencephaly type 1, lissencephaly type 1 due to doublecortin gene mutation, lissencephaly, X-linked, lissencephaly, X-linked, type 1, subcortical laminal heterotopia, X-linked, Dc syndrome, Double cortex syndrome, LISX

0 clinical trials for this condition and its sub-types, 0 tagged with Lissencephaly type 1 due to doublecortin gene mutation itself.

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↑ Classic lissencephaly (0) ↑ Subcortical band heterotopia (0)

Including sub-types (0) Tagged with Lissencephaly type 1 due to doublecortin gene mutation (0)

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