Duchenne muscular dystrophy is a genetic disorder that primarily affects males, but females can also be carriers of the gene mutation. While females typically do not show symptoms of the disease, they can experience muscle weakness and other complications. The challenges for females include the risk of passing the gene mutation to their children and the emotional burden of having family members affected by the disease. Additionally, females may face difficulties in accessing appropriate medical care and support services due to the focus on males in research and treatment.
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