Exp Neurobiol 2003; 12(2): 71-80
Published online December 31, 2003
© The Korean Society for Brain and Neural Sciences
Chang-Ho Yun1,* and Beom S. Jeon2
1Department of Neurology, College of Medicine, Inha University, Incheon 400-711, Korea, 2Department of Neurology, Seoul National University, College of Medicine, Seoul 110-744, Korea
Correspondence to: *To whom correspondence should be addressed.
TEL: 032-890-3418, FAX: 032-890-3864
The importance of genetic contributions to the epilepsies is now well established. Mutations in over 70 genes now define biological pathways leading to the epilepsy. These mutations disrupt a very large spectrum of biologic function. Some of the inherited errors alter the intrinisic ion channel properties directly responsible for neuronal hyperexcitability and others have impact on the brain development or cellular regulation. This paper reviews the pathogenic implications of the established genetic mutations and briefly mentioned the susceptible genes in hereditary or familial epilepsy syndrome.
Keywords: Genetic, epilepsy