Each form of muscular dystrophy has its own set of symptoms, but the underlying cause is similar: mutations in genes that are essential for muscle function. These mutations can be inherited from one or both biological parents, and this is why MD presents in a variety of forms. The severity and progression of symptoms depend on the type of muscular dystrophy and the specific genetic mutation involved. As muscular dystrophy is a progressive disorder, early diagnosis and intervention are crucial to managing the symptoms and improving quality of life.
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