Sponsored diagnostic testing programs for Restrictive Cardiomyopathy (RCM)
Restrictive Cardiomyopathy (RCM) is a rare form of cardiomyopathy in which the heart’s ventricles become abnormally stiff, limiting their ability to fill properly while maintaining normal contraction strength. This leads to symptoms such as fatigue, exercise intolerance, swelling, and signs of heart failure. RCM is often genetic and may be associated with infiltrative or storage disorders, making genetic testing an important part of evaluation.
1 program found for Restrictive Cardiomyopathy (RCM)
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.
