By detecting genetic mutations, the FAMILION tests can be used to recognize inherited forms of cardiac channelopathies or cardiomyopathies in individuals and their families and guide treatment to prevent the deadly cardiac events they can cause.

For cardiac channelopathies or cardiomyopathies that have already been diagnosed, the test can help doctors and patients make more informed treatment decisions and determine whether other family members may be at risk.

Patients and Family Members: Information about cardiac channelopathies, cardiomyopathies, frequently asked questions, Long QT Syndrome, Brugada Syndrome, Catecholaminergic Polymorphic Ventricular Tachycardia, HCM or resources, and more.

Physicians and Healthcare Providers: Instructions for ordering and administering FAMILION, technical specifications, and other resources for health care providers.

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