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.
(c) 2006 Wiley-Liss, Inc.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Epilepsy, Absence / genetics
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Epilepsy, Generalized / genetics*
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Epilepsy, Temporal Lobe / genetics
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Genetic Linkage
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Humans
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Models, Animal
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Mutation
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NAV1.1 Voltage-Gated Sodium Channel
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NAV1.2 Voltage-Gated Sodium Channel
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Nerve Tissue Proteins / chemistry
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Nerve Tissue Proteins / genetics
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Protein Structure, Tertiary
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Protein Subunits / chemistry
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Protein Subunits / genetics
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Receptors, GABA-A / chemistry
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Receptors, GABA-A / genetics*
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Seizures, Febrile / genetics*
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Sodium Channels / chemistry
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Sodium Channels / genetics*
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Syndrome
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Voltage-Gated Sodium Channel beta-1 Subunit
Substances
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NAV1.1 Voltage-Gated Sodium Channel
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NAV1.2 Voltage-Gated Sodium Channel
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Nerve Tissue Proteins
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Protein Subunits
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Receptors, GABA-A
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SCN1A protein, human
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SCN1B protein, human
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SCN2A protein, human
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Sodium Channels
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Voltage-Gated Sodium Channel beta-1 Subunit
Associated data
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OMIM/121210
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OMIM/604233
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OMIM/607208