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Duchenne Muscular Dystrophy (DMD)

What is Duchenne Muscular Dystrophy (DMD)?

The term muscular dystrophy refers to a group of over 30 disorders that affect the muscles. Duchenne muscular dystrophy is one type of muscular dystrophy that occurs primarily in boys.

Duchenne Muscular Dystrophy Care at Stanford

Early, accurate diagnosis and targeted treatments are crucial for helping children with Duchenne muscular dystrophy. Our Neuromuscular Program doctors have diagnosed hundreds of cases of Duchenne muscular dystrophy over the years. They often pick up on subtle signs of Duchenne other doctors may miss. This expertise helps lead to rapid diagnosis.

Our Neuromuscular Program holds the distinction of receiving an MDA Clinic designation in California. Learn more about the expertise of our team at the Neuromuscular Program.

What are the Symptoms of Duchenne Muscular Dystrophy?

Because Duchenne progresses rapidly, it is important to get an accurate diagnosis as soon as possible. Read more about the signs and symptoms of duchenne muscular dystrophy.

How is Duchenne Muscular Dystrophy Treated?

At Stanford, each child's symptoms and treatment needs are unique, and we tailor our care plan to address your child's specific situation. Treatment may include medications, counseling and a number of therapy options.

Learn more about duchenne muscular dystrophy treatment at Stanford.

Clinical Trials for Duchenne Muscular Dystrophy (DMD)

Clinical trials are research studies that evaluate a new medical approach, device, drug, or other treatment. As a Stanford Health Care patient, you may have access to the latest, advanced clinical trials.

Open trials refer to studies currently accepting participants. Closed trials are not currently enrolling, but may open in the future.

Open Trials Closed Trials