Whole gene duplication of SCN2A and SCN3A is associated with neonatal seizures and a normal intellectual development

Duplications at 2q24.3 encompassing the voltage‐gated sodium channel gene cluster are associated with early onset epilepsy. All cases described in the literature have presented in addition with different degrees of intellectual disability, and have involved neighbouring genes in addition to the sodi...

Full description

Saved in:
Bibliographic Details
Published in:Clinical genetics Vol. 91; no. 1; pp. 106 - 110
Main Authors: Thuresson, A‐C., Van Buggenhout, G., Sheth, F., Kamate, M., Andrieux, J., Clayton Smith, J., Soussi Zander, C.
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-01-2017
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Duplications at 2q24.3 encompassing the voltage‐gated sodium channel gene cluster are associated with early onset epilepsy. All cases described in the literature have presented in addition with different degrees of intellectual disability, and have involved neighbouring genes in addition to the sodium channel gene cluster. Here, we report eight new cases with overlapping duplications at 2q24 ranging from 0.05 to 7.63 Mb in size. Taken together with the previously reported cases, our study suggests that having an extra copy of SCN2A has an effect on epilepsy pathogenesis, causing benign familial infantile seizures which eventually disappear at the age of 1–2 years. However, the number of copies of SCN2A does not appear to have an effect on cognitive outcome. Whole gene duplications of SCN2A causes benign familial infantile seizures, but does not affect cognitive outcome.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0009-9163
1399-0004
1399-0004
DOI:10.1111/cge.12797