Genetics of Epilepsy

Author:

Willmore L. James1,Ueda Yuto2

Affiliation:

1. Departments of Neurology and Pharmacology and Physiology, Saint Louis University School of Medicine, St. Louis, MO, willmore@slu.edu.

2. Department of Psychiatry, Miyazaki Medical College, Miyazaki, Japan

Abstract

Understanding the molecular biology of epilepsy is a challenge for modern science. Epilepsy results from alternations in fundamental mechanisms of brain and membrane function. Although an understanding of the mode of inheritance and the etiology of genetic epilepsy syndromes forms the basis for genetic counseling, the development of specific therapies will come from knowing the basic mechanisms of epilepsy. Defining the genes causing epilepsy requires an unambiguous definition of seizure phenotype, along with the stability of that trait, an unremitting clinical course, and an abundance of clinical material. This article reviews the task of defining the genetics of epilepsy and discusses genetic methodology, idiopathic generalized and localization-related partial epilepsies, neuronal migration disorders, progressive myoclonus epilepsies, molecular biology of epileptogenesis, and future research. (J Child Neurol 2002;17:S18—S27).

Publisher

SAGE Publications

Subject

Clinical Neurology,Pediatrics, Perinatology, and Child Health

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy;Frontiers in Neuroscience;2023-05-12

2. Temporal Lobe Epilepsy in Children;Epilepsy Research and Treatment;2012-10-20

3. PEDIATRIC EPILEPSY SYNDROMES;CONTINUUM: Lifelong Learning in Neurology;2010-06

4. Introduction to Epilepsy;Magnetic Resonance in Epilepsy;2005

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