Genes and loci involved in febrile seizures and related epilepsy syndromes

被引:46
作者
Audenaert, D
Van Broeckhoven, C
De Jonghe, P
机构
[1] Univ Antwerp VIB, Dept Mol Genet, Neurogenet Grp, B-2610 Antwerp, Belgium
[2] Univ Antwerp Hosp, Div Neurol, Antwerp, Belgium
关键词
febrile seizures; generalized epilepsy with febrile seizures plus; ion channels; linkage; SCN1B; SCN1A; SCN2A; GABRG2; GABRG; GABRD; VLGR1; IMPA2;
D O I
10.1002/humu.20279
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Epilepsy is a paroxysmal disorder with a cumulative incidence of about 3%. About 13% of patients with epilepsy have a history of febrile seizures (FS). Generalized epilepsy with FS plus (GEFS+) is a familial epilepsy syndrome in which patients can have classic FS, FS that persist beyond the age of 5 years (i.e., FS+), and/or epilepsy. Both genetic and environmental factors have been shown to contribute to the pathogenesis of FS and GEFS+. During the past 10 years, molecular genetic studies have contributed a great deal to the identification of genetic factors involved in FS and GEFS+. In this study we aimed to provide a comprehensive review of currently known genes for FS and GEFS+, and the methods and approaches used to identify them. We also discuss the knowledge we currently have and hypotheses regarding the effect of the mutations on their respective protein functions.
引用
收藏
页码:391 / 401
页数:11
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