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) [22] …

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 absence of the …

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 chromosomes, …

Dec 8, 2025 · Dyne Therapeutics Announces Positive Topline Results from Phase 1/2 DELIVER Trial of Z-Rostudirsen in Duchenne Muscular Dystrophy (DMD)

Duchenne muscular dystrophy (DMD) affects the muscles, leading to muscle wasting that gets worse over time. DMD occurs primarily in males, though in rare cases may affect females. The symptoms …

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

6 days ago · It usually first appears in childhood. DMD is more common in boys due to its X-linked genetic inheritance pattern. There is no cure for DMD, and it is a progressive disease that often leads …

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 significant challenges.