Pediatric Muscular Dystrophy

Pediatric muscular dystrophy is a group of genetic disorders that cause progressive weakness and degeneration of muscle tissue in children. These conditions result from mutations that affect proteins essential for maintaining healthy muscle fibers. As muscles weaken over time, children may experience difficulty walking, climbing stairs, or performing everyday activities. There are different types, with Duchenne muscular dystrophy being the most common and severe. Although there’s no cure yet, treatments focus on managing symptoms, improving strength, and maintaining mobility through therapies, medications, and supportive devices. Early diagnosis and ongoing care can enhance quality of life for affected children.