CASE DISCUSSION
Pediatric Muscular Dystrophy
Presented from India by Dr. Rama Krishna Cheruvu0
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Case Description
Pediatric muscular dystrophy is a group of genetic disorders characterized by progressive muscle weakness and degeneration in children. The most common type, Duchenne muscular dystrophy (DMD), typically manifests in early childhood, often between the ages of 2 and 5. Children with this condition...
Case Summary
- Muscular dystrophy is a rare genetic neuromuscular disorder caused by defects in muscle proteins, leading to muscle weakness and difficulty in movement. The incidence is around 10 to 20 per one lakh population, with over 75 different types identified. Diagnosis requires identifying a primary myopathy with a genetic basis, progressive course, and muscle fiber degeneration on biopsy.
Speaker Profile
Dr. Rama Krishna Cheruvu
Alumni- Sikkim Manipal UniversitySenior Consultant Pediatrician, Mayflower Hospital & Trinity Hospital, Hyderabad
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