catecholaminergic polymorphic ventricular tachycardia 2

A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the CASQ2 gene on chromosome 1p13.

Signs and symptoms

• Syncope
• Polymorphic ventricular tachycardia
• Bradycardia
• Seizure
• Ventricular tachycardia
• Sudden death

Also known as: CVPT2