Lifelong management is required; no cure currently exists
Duchenne muscular dystrophy is a genetic disorder characterized by progressive muscle degeneration and weakness. It primarily affects boys. Management involves supportive care, physical therapy, and, in some cases, medications.
Progressive muscle degeneration leading to weakness and loss of function
Muscle weakness, difficulty walking
Genetic testing, clinical evaluation
Variable, can lead to loss of ambulation and respiratory complications
Muscle weakness, complications affecting mobility
Genetic mutations (X-linked recessive)
Physical therapy, medications, supportive care
Physical therapy, medications, supportive care
Genetic disorder characterized by progressive muscle degeneration and weakness
Supportive care, physical therapy, sometimes medications
While the information presented here reflects the current knowledge about these conditions and treatments, it’s important to understand that individual cases may differ. Consulting with a healthcare professional is crucial for accurate information tailored to your specific needs.
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