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Duchenne Muscular Dystrophy: Symptoms, Causes, and Treatment
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Duchenne Muscular Dystrophy (DMD) is one of the most severe and common types of muscular dystrophy, primarily affecting boys in early childhood. Characterized by progressive muscle weakness and degeneration, this genetic disorder impacts every aspect of life—from mobility and heart function to respiratory health and emotional well-being. Though it currently has no cure, advancements in research and treatment are helping patients live longer, more fulfilling lives than ever before.
Understanding the full scope of DMD—including its symptoms, genetic causes, diagnostic process, and current treatment options—is essential for affected families, caregivers, educators, and medical professionals. This guide will walk you through everything you need to know about Duchenne Muscular Dystrophy, offering a clear and compassionate overview of what to expect and how to manage this challenging condition.