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, …

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 …

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.

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

Jul 14, 2023 · There are nine types of muscular dystrophy. Duchenne muscular dystrophy (DMD) is the most common type of muscular dystrophy. It’s also one of the most severe, worsening more rapidly …

Nov 29, 2023 · DMD is one of the most common and severe forms of muscular dystrophy. It primarily affects young males. This article outlines the causes, symptoms, treatment, and outlook for DMD.