Myoclonic epilepsy evolved into West syndrome: a patient with a novel de novo KCNQ2 mutation

Acta Neurol Belg. 2015 Sep;115(3):475-8. doi: 10.1007/s13760-014-0344-5. Epub 2014 Aug 5.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Electroencephalography
  • Epilepsies, Myoclonic / genetics*
  • Epilepsies, Myoclonic / physiopathology
  • Humans
  • Infant
  • KCNQ2 Potassium Channel / genetics*
  • Male
  • Mutation, Missense
  • Spasms, Infantile / genetics*
  • Spasms, Infantile / physiopathology

Substances

  • KCNQ2 Potassium Channel
  • KCNQ2 protein, human