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