Conditions / Genetic
catecholaminergic polymorphic ventricular tachycardia 4
info · Genetic · ICD-10: I47.2
A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the CALM1 gene on chromosome 14q32.
Signs and symptoms
- Premature ventricular contraction
- Syncope
- Vertigo
- Ventricular tachycardia
- Sudden cardiac death
- Ventricular fibrillation
- Cardiac arrest
Also known as: CVPT4