Emery-Dreifuss muscular dystrophy (EDMD)

Sponsored diagnostic testing programs for Emery-Dreifuss muscular dystrophy (EDMD)

Emery-Dreifuss Muscular Dystrophy (EDMD) is a hereditary neuromuscular disorder marked by early-onset joint contractures, progressive muscle weakness, and cardiac conduction abnormalities. Symptoms often begin in childhood or adolescence, with many patients developing potentially serious heart rhythm issues that require ongoing monitoring and management.

1 program found for Emery-Dreifuss muscular dystrophy (EDMD)

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
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Performing labInvitae | Labcorp