Conditions / Genetic
long QT syndrome 15
info · Genetic · ICD-10: I45.8
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the CALM2 gene on chromosome 2p21.
Signs and symptoms
- Prolonged QTc interval
- 2:1 atrioventricular block
- Sinus bradycardia
- Syncope
- Bradycardia
- Cardiac arrest
- Premature ventricular contraction
- Ventricular fibrillation
- Seizure
- Left ventricular noncompaction
Also known as: LQT15