Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare inherited cardiac
ion channelopathy where the initial disease presentation is during childhood or adolescent …

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a highly malignant
inheritable cardiac channelopathy. The past decade and a half has provided exciting new …

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare and potentially
lethal inherited arrhythmia disease characterized by exercise or emotion-induced …

Aims Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an ion
channelopathy characterized by ventricular arrhythmia during exertion or stress. Mutations …

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe hereditary
arrhythmia syndrome predominantly affecting children and young adults. It manifests …

Background Catecholaminergic polymorphic ventricular tachycardia (CPVT) is often a life-
threatening arrhythmia disorder with variable penetrance and expressivity. Little is known …

Background—Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a lethal,
rare hereditary disease with an estimated prevalence of 1: 10 000. The genetic variants that …

CPVT is usually related to RyR2 or associated proteins. Emerging studies reveal several
genotype–phenotype correlations, which may eventually influence therapeutic decision …

In this final of a 5-part Focus Seminar series on precision medicine, we focus on
catecholaminergic polymorphic ventricular tachycardia (CPVT). This focus on CPVT allows …

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited
channelopathy. In this review, we summarize the epidemiology, pathophysiology, clinical …