Physicians and Healthcare Providers

FAMILION opens new options in the diagnosis of cardiac channelopathies and cardiomyopathies including LQTS, Brugada Syndrome, CPVT and HCM.  The FAMILIONfamily of tests can:

• Analyze specific ion channel genes to detect the mutations that cause cardiac channelopathies
• Help diagnose LQTS, Brugada Syndrome, CPVT, HCM and other associated disorders before patients exhibit symptoms
• Help determine the cause of the disorder
• Help determine whether a patient’s family members have the same mutation
• Guide treatment options and medication choices

It’s a simple test that’s leading to reduced uncertainty and more sophisticated diagnoses of cardiac channelopathies and cardiomyopathies. That’s the value of FAMILION.

FAQs
Frequently asked questions about how FAMILION works and how it can be used to guide the course of treatment.

Technical Specifications
The science behind the FAMILION test

Resources
Study references and links to outside organizations that deal with LQTS, Brugada Syndrome, CPVT, HCM and associated disorders.

Ordering
How to order a test kit.

Test Instructions

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