Pediatric Neurology Briefs (Mar 1999)

Double Cortex Syndrome

  • J Gordon Millichap

DOI
https://doi.org/10.15844/pedneurbriefs-13-3-1
Journal volume & issue
Vol. 13, no. 3
pp. 17 – 18

Abstract

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The incidence of mutations in the X-linked gene doublecortin in patients with “double cortex” syndrome (DC; also called subcortical band heterotopia or laminar heterotopia) and familial DC with lissencephaly was investigated in a cohort of 8 pedigrees and 47 sporadic patients with DC examined at the Division of Neurogenics, Beth Israel Deaconess Medical Center, Boston, and multiple centers in the US and abroad.

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