Duchenne muscular dystrophy is a rare progressive disease that eventually affects all voluntary muscles and involves the heart and breathing muscles in later stages.

It’s the most common form of muscular dystrophy and the leading type of severe inherited muscle disorder (myopathies). While there’s no cure, and it will shorten life expectancy, treatments are …

Jul 10, 2023 · Duchenne muscular dystrophy (DMD) is one of the most severe forms of inherited muscular dystrophies. It is the most common hereditary neuromuscular disease and does not …

Duchenne muscular dystrophy, or DMD, is associated with the most severe clinical symptoms of all the muscular dystrophies. It is caused by a genetic mutation on one of the mother’s X …

Apr 18, 2013 · Boys with Duchenne muscular dystrophy do not make the dystrophin protein in their muscles. Duchenne muscular dystrophy affects approximately 1 in 3500 male births …

2 days ago · Duchenne muscular dystrophy is a progressive, usually fatal, genetic disorder that causes muscle weakness. Find out more.

Dec 4, 2025 · It’s caused by a lack of a protein called dystrophin. This causes muscle fibres to break down. They’re replaced by fibrous or fatty tissues that cause the muscle to gradually …

Duchenne muscular dystrophy is the most common type of muscular dystrophy. It causes progressive muscle weakness and eventually leads to an inability to walk. It also can weaken …

Duchenne muscular dystrophy (DMD) is a progressive, genetic (X-linked recessive) neuromuscular disorder caused by mutations to the DMD gene, resulting in the dysfunction or …

What is Duchenne muscular dystrophy? Duchenne muscular dystrophy (DMD) is a type of muscular dystrophy, a rare genetic disorder that causes muscles to become weak and waste …