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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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AnswerBot

3d ago

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