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Duchenne Muscular Dystrophy (DMD): What It Is Symptoms - Cleveland Clinic 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 The disease mainly affects boys There currently isn’t a cure Treatment involves managing symptoms and improving quality of life
Duchenne muscular dystrophy - Wikipedia Microscopic image of cross-sectional calf muscle from a person with Duchenne muscular dystrophy, showing extensive replacement of muscle fibers by fat cells
Duchenne Muscular Dystrophy - Johns Hopkins Medicine 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, and researchers have identified some of the affected genes
Types of Muscular Dystrophy - CDC 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 progresses more quickly than BMD About 14 in 100,000 males aged 5–24 years of age are affected 1 Males are more likely to be affected than females
Duchenne Muscular Dystrophy - Nationwide Childrens Hospital Duchenne muscular dystrophy (DMD) is a rare condition defined by worsening muscle weakness and damage It is the most common inherited neuromuscular disorder that affects all races and ethnicities DMD only affects males and children with DMD may lose the ability to walk as early as 7 years of age
Duchenne muscular dystrophy | About the Disease | GARD 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 of DMD include progressive weakness and loss (atrophy) of both skeletal and heart muscle
DMD Patients: An Overview of Signs, Diagnosis, and Care Levels in DMD patients are typically 50 to 200 times higher than normal Confirmation of DMD primarily relies on genetic testing, which identifies specific mutations within the DMD gene In rare cases where genetic testing is inconclusive, a muscle biopsy may be performed to analyze the presence or absence of dystrophin protein in muscle tissue