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- Living with DMD

Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness. It is one of nine types of muscular dystrophy. DMD is caused by an absence of dystrophin, a protein that helps keep muscle cells intact. Symptom onset is in early childhood, usually between ages 3 and 5. The disease primarily affects boys, but in rare cases it can affect girls.

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Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness. It is one of nine types of muscular dystrophy. DMD is caused by an absence of dystrophin, a protein that helps keep muscle cells intact. Symptom onset is in early childhood, usually between ages 3 and 5. The disease primarily affects boys, but in rare cases it can affect girls.
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- Living with DMD | livingwithdmd.org Reviews

https://livingwithdmd.org

Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness. It is one of nine types of muscular dystrophy. DMD is caused by an absence of dystrophin, a protein that helps keep muscle cells intact. Symptom onset is in early childhood, usually between ages 3 and 5. The disease primarily affects boys, but in rare cases it can affect girls.

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Living with DMD » Blog

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Living with DMD » LEJOG

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26/07/2015 00:00 - 00:00. Lands End - John O'Groats. I will be cycling from Land's End to John O'Groats for Action Duchenne. Because we need to raise awareness and funds for (DMD). My little boy Dylan now 5 was diagnosed with Duchenne Muscular Dystrophy (DMD) just as he turned 2 years old. DMD is 100% fatal there is no cure, the only drug that can be used is steroids, and that is only to keep them mobile and help with respiratory functions for as long as possible, but has well documented side affects.

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Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness. It is one of nine types of muscular dystrophy. DMD is caused by an absence of dystrophin, a protein that helps keep muscle cells intact. Symptom onset is in early childhood, usually between ages 3 and 5. The disease primarily affects boys, but in rare cases it can affect girls.

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