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DMD, or Duchenne Muscular Dystrophy, is a genetic disorder characterized by progressive muscle degeneration and weakness due to the absence of dystrophin, a protein essential for muscle fiber integrity. It primarily affects boys, typically beginning in early childhood, and leads to significant mobility issues and eventual loss of muscle function. The condition is caused by mutations in the DMD gene located on the X chromosome, making it X-linked recessive. Management often involves physical therapy, corticosteroids, and supportive care, but there is currently no cure.

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Muscular dystrophy, particularly Duchenne muscular dystrophy (DMD), is an X-linked recessive genetic disorder. This means that the gene responsible for DMD is located on the X chromosome, and males, having only one X chromosome, are more severely affected. In contrast, females can be carriers and may show mild symptoms if they have one affected X chromosome. Incomplete dominance is a different genetic concept and does not apply to muscular dystrophy.


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