Sponsored diagnostic testing programs for Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) is a rare, inherited arrhythmia disorder characterized by stress- or exercise-induced episodes of rapid, irregular heartbeats. These arrhythmias can lead to dizziness, fainting, or sudden cardiac arrest, often in otherwise healthy children or young adults. CPVT is highly treatable when identified early, making timely diagnosis critical.
1 program found for Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)
The Invitae Unlock™ Cardiomyopathy & Arrhythmia program offers no-charge genetic testing for U.S. patients with suspected inherited cardiomyopathy or arrhythmia. The comprehensive panel supports diagnostic clarification, risk assessment, and family variant identification. Eligible patients may access testing at no cost when ordered by a qualified healthcare provider.
