No cure; treatment focuses on managing symptoms, preserving function, and improving quality of life; outcomes vary based on the severity of the condition
Becker muscular dystrophy is a genetic disorder that causes progressive muscle weakness and wasting. It is related to Duchenne muscular dystrophy but tends to have a later onset and a milder course. Treatment focuses on managing symptoms and maintaining mobility.
Genetic disorder causing progressive muscle weakness and wasting
Progressive muscle weakness, difficulty walking, muscle wasting
Genetic testing, muscle biopsy
Variable; generally milder than Duchenne muscular dystrophy
Progressive muscle weakness, complications in severe cases
Mutation in the DMD gene, leading to a deficiency in the dystrophin protein
Supportive care, physical therapy, assistive devices, sometimes corticosteroids or other medications
Supportive care, physical therapy, assistive devices, sometimes corticosteroids or other medications
X-linked genetic disorder affecting muscle function
Multidisciplinary care for symptom management and supportive interventions
This information is for general understanding and is not a substitute for professional medical advice. Always consult with healthcare providers for accurate and personalized information related to your health.
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