Conditions / Genetic
long QT syndrome 5
info · Genetic · ICD-10: I45.8
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNE1 gene on chromosome 21q22.12.
Signs and symptoms
- Sinus bradycardia
- Prolonged QTc interval
- Ventricular fibrillation
- Syncope
- Torsade de pointes
- Sudden cardiac death
Also known as: LQT5