Duchenne muscular dystrophy (DMD) is a condition that causes skeletal and heart muscle weakness that quickly gets worse with time. Symptoms usually begin by age 6.

DMD is inherited in an X-linked recessive manner. Duchenne muscular dystrophy is caused by a mutation of the dystrophin gene, located on the short arm of the X chromosome (locus Xp21) …

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 …

Jan 8, 2026 · Code lookup Search by ATC, GTIN, Pack or Product Order Number and SNOMED code.

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 …

Duchenne muscular dystrophy (DMD) is a severe, progressive, and ultimately fatal disease of skeletal muscle wasting, respiratory insufficiency, and cardiomyopathy.

Apr 18, 2013 · What is Duchenne muscular dystrophy? DMD is a rapidly progressive form of muscular dystrophy that occurs primarily in boys.

Nov 4, 2025 · Duchenne muscular dystrophy (DMD) is a rare muscle weakening disease that mostly affects boys. Learn about the causes, symptoms, treatment, and other parts of …

Feb 20, 2025 · Duchenne muscular dystrophy (DMD) is a rare neurological condition that causes severe muscular weakness and mild intellectual disability.

Duchenne Muscular Dystrophy, often abbreviated as DMD, is a progressive and severe muscle-wasting condition. Individuals diagnosed with DMD, a form of muscular dystrophy, face …