Becker Muscular Dystrophy (BMD)

Sponsored diagnostic testing programs for Becker Muscular Dystrophy (BMD)

Becker muscular dystrophy (BMD) is an X-linked neuromuscular disorder caused by changes in the DMD gene that reduce or alter dystrophin, a protein that stabilizes muscle cells. It typically presents later and progresses more slowly than Duchenne, with proximal muscle weakness and calf enlargement. Cardiac involvement (dilated cardiomyopathy, arrhythmias) is common and warrants ongoing monitoring.

1 program found for Becker Muscular Dystrophy (BMD)

Programs

1 program
Duchenne Muscular Dystrophy (DMD)Becker Muscular Dystrophy (BMD)
Decode Duchenne
Sponsored by
Parent Project Muscular Dystrophy
Sarepta Therapeutics

Comprehensive DMD testing

Decode Duchenne provides sponsored, no-cost diagnostic testing for suspected Duchenne/Becker muscular dystrophy in patients residing in the U.S. or Canada. The program is administered with Parent Project Muscular Dystrophy and performed by Revvity Omics; industry partners (e.g., Sarepta and others) provide support. Order per clinical presentation; genetic counseling resources are available.

Musculoskeletal
ViewOrder
Performing labRevvity Omics, Inc.