Conditions / Genetic
long QT syndrome 2
info · Genetic · ICD-10: I45.8
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1.
Signs and symptoms
- Prolonged QT interval
- Prolonged QTc interval
- Notched T wave
- Syncope
- Ventricular fibrillation
- Torsade de pointes
- Sudden cardiac death
- Cardiac arrest
Also known as: LQT2