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 is extremely rare in females (about 1 in 50,000,000 female births). [6] It can occur in females with an affected father and a carrier mother, in those who are missing an X …

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 …

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 managing DMD.

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, …

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 …

Understand the signs, symptoms and stages of Duchenne muscular dystrophy (DMD), and how the genetic disease is inherited and diagnosed.

Duchenne and Becker muscular dystrophies have similar signs and symptoms and are caused by different mutations in the same gene. The two conditions differ in their severity, age of onset, and …

Duchenne muscular dystrophy is caused by a defective gene for dystrophin (a protein in the muscles). However, it often occurs in people without a known family history of the condition. The condition most …

Duchenne muscular dystrophy is a rare, genetic condition that is characterized by progressive muscle damage and weakness. Sometimes shortened to DMD or Duchenne, this rare disease is caused by …