Living with a rare form of muscular dystrophy, and being honoured with having the youngest-ever seat on the board of trustees ...

A rare and fatal form of muscular dystrophy has long posed a devastating diagnosis for children, primarily affecting boys.

A 46-year-old woman with type 1 myotonic dystrophy (DM1) presented to the emergency department with dyspnea and palpitations.

Delandistrogene moxeparvovec, a gene therapy for Duchenne muscular dystrophy (DMD), showed high dystrophin expression and a ...

Firefighters will be in Capitola Village this weekend accepting donations on behalf of the Muscular Dystrophy Association ...

No clinically significant changes were observed on physical examination, in vital signs, or on electrocardiograms ... in patients with Duchenne's muscular dystrophy. No serious adverse events ...

Duchenne muscular dystrophy (DMD), recognised by the World ... neurologist and epileptologist, Medical Trust Hospital, Kochi, early signs of DMD include delays in walking, toe walking, stiffness ...

Meghana Keshavan covers biotech and contributes to The Readout newsletter. Want to stay on top of the science and politics driving biotech today? Sign up to get our biotech newsletter in your inbox.

Building on its 75-year legacy of progress, MDA is reinforcing its commitment to the ALS community by driving momentum for treatments and expanding access to multidisciplinary care. "Eleanor Gehrig's ...

The condition is named for the German physician Peter Emil Becker, who first described this variant of muscular dystrophy in the 1950s. What are the signs and symptoms of Becker muscular dystrophy?

today announced initial Phase 1 data in an oral presentation at the 2025 Muscular Dystrophy Association (MDA) Clinical & Scientific Conference in Dallas, Texas. "We are very pleased by these early ...

FILE - A sign for the U.S. Food and Drug Administration ... died while taking its closely watched gene therapy for muscular dystrophy, sending company shares plummeting more than 25%.