Syndactyly and long QT syndrome (CaV1.2 missense mutation G406R) is associated with hypertrophic cardiomyopathy

Heart Rhythm. 2005 Dec;2(12):1365-8. doi: 10.1016/j.hrthm.2005.08.024.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Calcium Channels, L-Type / genetics
  • Cardiomyopathy, Hypertrophic / complications*
  • Cardiomyopathy, Hypertrophic / genetics
  • Heart Block / complications
  • Heart Block / genetics
  • Humans
  • Infant, Newborn
  • Long QT Syndrome / complications*
  • Long QT Syndrome / genetics
  • Male
  • Mutation, Missense
  • Sepsis / complications
  • Syndactyly / complications*
  • Syndactyly / genetics
  • Syndrome
  • Systole
  • Tachycardia, Ventricular / complications
  • Tachycardia, Ventricular / genetics
  • Ventricular Dysfunction, Left / complications
  • Ventricular Dysfunction, Left / genetics

Substances

  • Calcium Channels, L-Type