Double Cortex Syndrome

J Gordon Millichap

doi:10.15844/pedneurbriefs-13-3-1

Double Cortex Syndrome

Pediatric Neurology Briefs

Volume 13 (1999): Issue 3

By: J Gordon Millichap

Open Access

|Mar 1999

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.

References

Gleeson JG Minnerath SR Fox JW Allen KM Luo RF Hong SE Characterization of mutations in the gene doublecortin in patients with double cortex syndrome Ann Neurol 1999 Feb 45 2 146 153 10.1002/1531-8249(199902)45:2<;146::AID-ANA3>3.0.CO;2-N 9989615
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Fogli A Guerrini R Moro F Fernandez-Alvarez E Livet MO Renieri A Intracellular levels of the LIS1 protein correlate with clinical and neuroradiological findings in patients with classical lissencephaly Ann Neurol 1999 Feb 45 2 154 161 10.1002/1531-8249(199902)45:2<;154::AID-ANA4>3.3.CO;2-G 9989616
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-13-3-1 | Journal eISSN: 2166-6482

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Language: English

Page range: 17 - 18

Published on: Mar 1, 1999

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Double Cortex Syndrome,

Neuronal Migration Disorders,

Lissencephaly

© 1999 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 13 (1999): Issue 3