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.

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 …

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, 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, …

Jan 12, 2026 · 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 …

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 …

Sometimes shortened to DMD or Duchenne, this rare disease is caused by a genetic mutation that prevents the body from producing a protein called dystrophin. Dystrophin acts like a shock absorber …

Those affected usually maintain the ability to be able to use their hands to hold and use eating and writing utensils. All children with DMD will have some degree of intellectual impairment, with most …

Jan 7, 2025 · Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are caused by changes in the same gene. They have similar symptoms, but DMD is more severe and …

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