Novel mutation (H402R) in the S1 domain of KCNH2-encoded gene associated with long QT syndrome in a Spanish family

Int J Cardiol. 2010 Jul 9;142(2):206-8. doi: 10.1016/j.ijcard.2008.11.166. Epub 2009 Jan 10.

Abstract

Long-QT syndrome is a congenital cardiac disease resulting in ventricular arrhythmias and sudden death. Genetic mutations in two protein ion-channel genes, KCNQ1 and KCNH2. The mutations position in these genes provides additional information about the evaluation of the risk-stratification. In a Spanish family in whom previous repetitive syncope episodes, sudden death and pathological prolongation of the QT interval were documented, a novel heterozygous mutation in the KCNH2 gene (A1218>G) was identified. This mutation loading to amino acid substitution H420R in the S1 transmembrane domain of KCNH2. The new A1218>G mutation in the KCNH2 gene detected in this Spanish family causes arrhythmia manifestation in the carriers.

Publication types

  • Case Reports
  • Comparative Study
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Substitution / genetics*
  • Arginine / genetics
  • Arrhythmias, Cardiac / genetics
  • ERG1 Potassium Channel
  • Ether-A-Go-Go Potassium Channels / genetics*
  • Female
  • Genetic Carrier Screening
  • Histidine / genetics
  • Humans
  • Long QT Syndrome / diagnosis
  • Long QT Syndrome / epidemiology
  • Long QT Syndrome / genetics*
  • Male
  • Mutation, Missense / genetics*
  • Pedigree
  • Protein Structure, Tertiary / genetics
  • Spain / epidemiology

Substances

  • ERG1 Potassium Channel
  • Ether-A-Go-Go Potassium Channels
  • KCNH2 protein, human
  • Histidine
  • Arginine