Conditions / Genetic
long QT syndrome 6
info · Genetic · ICD-10: I45.8
A long QT interval syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE2 gene on chromosome 21q22.11.
Signs and symptoms
- Prolonged QTc interval
- Ventricular fibrillation
- Cardiac arrest
- Prolonged QT interval
- Syncope
- Sudden cardiac death
- Torsade de pointes
Also known as: LQT6