Dystrophinopathy

Sponsored diagnostic testing programs for Dystrophinopathy

Dystrophinopathy refers to a group of genetic muscle disorders caused by pathogenic variants in the DMD gene, leading to progressive muscle weakness. The spectrum includes Duchenne and Becker muscular dystrophies, which vary in severity and age of onset. Symptoms often involve difficulty walking, rising, or climbing stairs, with potential cardiac and respiratory involvement as the condition progresses.

1 program found for Dystrophinopathy

Programs

1 program
Invitae Unlock™

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

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.

Cardiology