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Genes and loci involved in febrile seizures and related epilepsy syndromes
Authors:Audenaert Dominique  Van Broeckhoven Christine  De Jonghe Peter
Affiliation:Department of Molecular Genetics, Neurogenetics Group, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Antwerp, Belgium.
Abstract:
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.
Keywords:febrile seizures  generalized epilepsy with febrile seizures plus  ion channels  linkage  SCN1B  SCN1A  SCN2A  GABRG2  GABRG  GABRD  VLGR1  IMPA2
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