What´s Duchenne Muscular Dystrophy?

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Duchenne Muscular Dystrophy Do you know what duchenne muscular dystrophy is? It obviously has something to do with your muscles it causes you to have muscle weakness which can lead you to have loss of mobility. This disease is most effective for males. Duchenne muscular dystrophy is a mutation, flaw or gene. It interferes with protein production that is needed to maintain and to form a healthy muscle. Duchenne muscular dystrophy symptoms are diagnosed according to where it is found in the body. It is usually caused by which gene you get. Duchenne muscular dystrophy is inherited. Treatment is mostly pain pills or treatment for mobility. Duchenne muscular dystrophy is found in males. The women can be carriers of the disease and pass it on to their sons and daughters but it is possible for the children not to be effected.

Origin of Discovery
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The disease is named after a man named Guillaume Benjamin Amand Duchenne in the 1860’s. Guillaume is a French neurologist. He described it to other scientists of his age and they went into deeper investigating. They found out that it only affects men. Women can be carriers. Carriers are women that have an X chromosome that has a duchenne muscular dystrophy gene.

Definition of Disorder The definition of duchenne muscular dystrophy (which includes what happens to the body and what part of the body does it generally affect) is an interfer with protein production that is needed to maintain and to form a healthy muscle. It is a mutation, flaw or gene. This disorder only affects males, women can be a carrier of the disorder but they are mostly not affected. Young boys with duchenne muscular dystrophy are normally latin learning to walk. The muscles are the most affected in the human body. Sometimes it causes you to have loss of mobility.

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