Duchenne muscular dystrophy (DMD) is a genetic condition ... With X-linked recessive inheritance, having only one copy of a gene alteration is sufficient to cause the condition in males.

Muscular dystrophy can appear in infancy up to middle age or later, and its form and severity are determined in part by the age at which it occurs. Some types of muscular dystrophy typically ...

In muscular dystrophy, the weakness is in the muscles. An inherited genetic mistake prevents the body from making a protein that helps build muscles and keep them strong. Only males can get ...

Research in genetics and biotechnology has advanced by leaps and bounds in recent years, offering new hope for the treatment ...

Use precise geolocation data and actively scan device characteristics for identification. This is done to store and access ...

While the last decade has brought considerable progress for patients with DMD, substantial unmet need remains. Several ...

For nearly 20 years, Spuler and her collaborators have been working to understand dysferlin, its role in muscular dystrophy and ways to cure these rare but devastating inherited diseases.

For nearly 20 years, Spuler and her collaborators have been working to understand dysferlin, its role in muscular dystrophy and ways to cure these rare but devastating inherited diseases. In the case ...

The FDA has granted fast track designation to DYNE-101, a therapy for myotonic dystrophy type 1 (DM1) now in testing in a ...

The rate of progression of the muscular dystrophies depends on the type of dystrophy. While some progress slowly, others confine the patient to a wheelchair within a few years. Significant advances in ...