[Recent insights into the implication of ion channels in familial forms of epilepsies associated or non associated to febrile convulsions]

Rev Neurol (Paris). 2004 May;160(5 Pt 2):S90-7. doi: 10.1016/s0035-3787(04)71011-5.
[Article in French]

Abstract

Major advances have recently been made in the understanding of the genetic bases of monogenic inherited epilepsies. For several idiopathic epilepsies, mutations in genes encoding subunits of ion channels or ligand receptors have been demonstrated. This is the case for some generalized idiopathic epilepsies and generalized epilepsies associated with febrile seizures. In this Article, we review the recent clinical and genetic data of these forms of epilepsy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • CLC-2 Chloride Channels
  • Child
  • Chloride Channels / genetics
  • Epilepsy / genetics*
  • Epilepsy / physiopathology*
  • Epilepsy, Generalized / genetics
  • Epilepsy, Generalized / physiopathology
  • Humans
  • Ion Channels / physiology*
  • Mutation / physiology
  • Myoclonic Epilepsy, Juvenile / genetics
  • Receptors, GABA-A / genetics
  • Seizures, Febrile / genetics*
  • Seizures, Febrile / physiopathology*

Substances

  • CLC-2 Chloride Channels
  • Chloride Channels
  • Ion Channels
  • Receptors, GABA-A