Muscular dystrophy is caused by mutations in the genes responsible for the structure and function of muscles. These genetic mutations prevent the cells from properly maintaining muscle strength, leading to progressive muscle weakness. The most common symptoms include muscle atrophy, difficulty walking or performing physical tasks, and irregular gaits like waddling or toe walking. Over time, individuals may experience joint stiffness, contractures, spasticity, and muscle pain. With various forms of muscular dystrophy, the progression of these symptoms can affect different muscles and parts of the body in unique ways.
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