No cure; management focuses on improving quality of life and addressing specific symptoms
Centronuclear myopathy is a rare genetic muscle disorder characterized by muscle weakness and abnormal positioning of the cell nuclei in muscle fibers. Severity can vary. Treatment focuses on managing symptoms and supportive care.
Rare genetic muscle disorder characterized by muscle weakness and atrophy
Muscle weakness, delayed motor milestones, respiratory difficulties
Genetic testing, muscle biopsy
Variable; depends on the specific type and complications
Muscle weakness, respiratory complications
Genetic mutations affecting various proteins involved in muscle function
Supportive care, physical therapy, respiratory support, sometimes genetic counseling and testing
Supportive care, physical therapy, respiratory support, sometimes genetic counseling and testing
Genetic muscle disorder affecting the central nuclei of muscle fibers
Supportive care and physical therapy for maintaining function
For personalized advice and care, always seek the assistance of healthcare professionals. This information is meant for general understanding and not as a replacement for professional medical advice.
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