Gene defects in idiopathic epilepsy

Rev Neurol (Paris). 1999 Jul;155(6-7):450-3.

Abstract

Idiopathic epilepsies are mainly due to genetic factors. In most cases the mode of inheritance is either oligogenic or multifactorial. Only a few rare idiopathic epilepsies are single gene disorders. Monogenic epilepsies offer the chance to identify genes/gene families which might also be involved in the aetiology of common forms of the disease. The genetic basis of two monogenic epilepsies have recently been identified: autosomal dominant nocturnal frontal lobe epilepsy and benign familial neonatal convulsions.

Publication types

  • Review

MeSH terms

  • Chromosomes, Human, Pair 20
  • Epilepsy / genetics*
  • Epilepsy, Frontal Lobe / genetics
  • Humans
  • Infant, Newborn
  • KCNQ2 Potassium Channel
  • Mutation*
  • Potassium Channels / genetics*
  • Potassium Channels, Voltage-Gated
  • Receptors, Nicotinic / genetics*
  • Seizures / genetics

Substances

  • KCNQ2 Potassium Channel
  • KCNQ2 protein, human
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • Receptors, Nicotinic