BC65.5 Catecholaminergic polymorphic ventricular tachycardia

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe genetic arrhythmogenic disorder of childhood characterised by adrenergically-induced ventricular tachycardia (bidirectional ventricular tachycardia and, less frequently, supraventricular tachycardia and atrial fibrillation) manifesting as syncope and sudden death.

synonyms

• Catecholaminergic polymorphic ventricular tachycardia
• Catecholaminergic polymorphic ventricular tachycardia due to RYR2 mutation
• Catecholaminergic polymorphic ventricular tachycardia due to Calsequestrin mutation

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