Conditions / Genetic
long QT syndrome 1
info · Genetic · ICD-10: I45.8
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.
Signs and symptoms
- Syncope
- Prolonged QTc interval
- Prolonged QT interval
- Ventricular fibrillation
- Torsade de pointes
- Sudden cardiac death
- Hearing abnormality
Also known as: LQT1; ventricular fibrillation with prolonged QT interval