Conditions / Genetic

long QT syndrome 13

info · Genetic · ICD-10: I45.8

A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNJ5 gene on chromosome 11q24.3.

Signs and symptoms

  • Palpitations
  • Syncope
  • Cardiac arrest
  • Prolonged QTc interval
  • Congestive heart failure
  • Permanent atrial fibrillation
  • Atrioventricular block
  • Pulmonary embolism
  • Torsade de pointes
  • Reduced left ventricular ejection fraction

Also known as: LQT13