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Table of contents
- Case study of duchenne muscular dystrophy in 2021
- Muscular dystrophy articles
- Muscular dystrophy case study answers
- Duchenne muscular dystrophy powerpoint
- Muscular dystrophy assessment
- Duchenne muscular dystrophy case presentation
- Muscular dystrophy: case study pdf
- Current research on muscular dystrophy
Case study of duchenne muscular dystrophy in 2021
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Muscular dystrophy articles
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Muscular dystrophy case study answers
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Duchenne muscular dystrophy powerpoint
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Muscular dystrophy assessment
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Duchenne muscular dystrophy case presentation
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Muscular dystrophy: case study pdf
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Current research on muscular dystrophy
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How did the baby boy get Duchenne muscular dystrophy?
Eventually the baby boy was diagnosed with Duchenne Muscular Dystrophy, an inherited disorder that causes rapidly progressive muscle weakness and wasting. It is linked to a defective gene for dystrophin (a protein in the muscles). However, it does occur in people without a known family history of the condition.
How is Duchenne Muscular Dystrophy related to Misko?
It is linked to a defective gene for dystrophin (a protein in the muscles). However, it does occur in people without a known family history of the condition. When Misko’s parents started to research the disease, they found nothing in their native language, Hungarian*.
When did the Misko Muscular Dystrophy Foundation start?
Created in 2008, the aim of the Misko Foundation is to make Misko’s life as “ordinary” as possible, while searching for a possible cure, together with other parents. The foundation would like to raise the funds necessary for Misko to receive the best possible care available.
Last Update: Oct 2021