The FAMILION tests detect mutations that can cause cardiac channelopathies and cardiomyopathies, rare, potentially lethal heart conditions, including Long QT Syndrome (LQTS), Brugada Syndrome (BrS) Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT), Hypertrophic Cardiomyopathy (HCM), Arrhythmogenic Right Ventricular Cardiomyopathy, and Dilated Cardiomyopathy (DCM). By reducing uncertainty and finding the specific causes of cardiac channelopathies, the test can:

• Help diagnose a patient's disease
• Guide treatment options
• Determine whether family members are at risk

1-877-2-PGXHEALTH (877-274-9432)