Conditions / Genetic
long QT syndrome 12
info · Genetic · ICD-10: I45.8
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21.
Signs and symptoms
- Prolonged QTc interval
- Syncope
- Ventricular fibrillation
- Torsade de pointes
Also known as: LQT12