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 …

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 …

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 …

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 …

Duchenne is classified under muscular dystrophies, genetic diseases marked by muscle weakness, with Duchenne being notably the most severe due to the absence of dystrophin, a …

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 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. …

Duchenne muscular dystrophy is a severe, progressive, muscle-wasting disease that leads to difficulties with movement and, eventually, to the need for assisted ventilation and premature …

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