Double Cortex Syndrome

Authors

  • J Gordon Millichap Northwestern University Feinberg School of Medicine

DOI:

https://doi.org/10.15844/pedneurbriefs-13-3-1

Keywords:

Double Cortex Syndrome, Neuronal Migration Disorders, Lissencephaly

Abstract

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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Published

1999-03-01

Issue

Vol 13, No 03 | Mar 1999

Section

Congenital Malformations

License

Copyright (c) 1999 The Author(s)

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