Duchenne Muscular Dystrophy (DMD) Explained: Symptoms, Causes, and Disease Progression
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YouTubeVB Anatomy Bytes
Duchenne Muscular Dystrophy (DMD) Explained: Symptoms, Causes, and Disease Progression
Duchenne muscular dystrophy (DMD) is a rare X-linked recessive genetic muscle disorder caused by a mutation in the dystrophin gene, leading to complete loss of the dystrophin protein — the key structure that protects muscle cells from damage. Without dystrophin, muscle fibers tear during contractions, causing progressive muscle weakness ...
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When Creed was diagnosed with Duchenne muscular dystrophy as a baby, the hospital that diagnosed him said there was nothing they could do for him. After months of research, Creed’s family brought him to Duke Children's Duchenne MD clinic where the team offered him something no one else had: hope. Meet Creed and hear his incredible story, and make your donation to support Radiothon at https://duke.is/supportmixradiothon25. Radiothon for Duke Children's is presented by Lenovo | MIX 101.5 WRAL-FM
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💡 What does “severe phenotype” mean in Duchenne muscular dystrophy (DMD)? When doctors talk about a phenotype, they’re referring to the way a condition shows up in someone’s body, the physical traits and symptoms that result from their genetics. In Duchenne, a severe phenotype usually means the condition progresses more quickly, often with earlier loss of abilities like walking, climbing stairs, or raising arms. This can also bring earlier complications with breathing, heart health, and other a
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