Conditions / Genetic

long QT syndrome 15

info · Genetic · ICD-10: I45.8

A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the CALM2 gene on chromosome 2p21.

Signs and symptoms

  • Prolonged QTc interval
  • 2:1 atrioventricular block
  • Sinus bradycardia
  • Syncope
  • Bradycardia
  • Cardiac arrest
  • Premature ventricular contraction
  • Ventricular fibrillation
  • Seizure
  • Left ventricular noncompaction

Also known as: LQT15