catecholaminergic polymorphic ventricular tachycardia 1

A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the RYR2 gene on chromosome 1q43.

Signs and symptoms

• Bidirectional ventricular tachycardia
• Syncope
• Effort-induced polymorphic ventricular tachycardia
• Sudden cardiac death
• Seizure
• Atrial standstill
• Reduced systolic function
• Ventricular tachycardia
• Paroxysmal atrial fibrillation
• Dilated cardiomyopathy

Also known as: CVPT1; arrhythmogenic right ventricular dysplasia 2