In the mild form, persons usually develop cataracts and experience mild muscle tone dysfunction (myotonia). They normally do not experience clinical manifestations until they reach 20 years of age
Muscular Dystrophy causes numerous effects on the body. Here are just a few: aniexty, balance, bladder dysfunction, bowel problems, depression, and fatigue.
Muscular dystrophy is a group of genetic disorders characterized by muscle weakening and wasting, while Duchenne muscular dystrophy (DMD) is a specific type of muscular dystrophy caused by mutations in the dystrophin gene. DMD is the most common and severe form of muscular dystrophy, typically affecting boys and leading to progressive muscle weakness and loss of function.
Muscular dytrophy is not spread it is heriditary.
The muscular Dystrophy do not maintain homeostasis.
Muscular Dystrophy Association was created in 1950.
Duchenne's muscular dystrophy
Duchenne Muscular Dystrophy
what are the goals fo rehabilitation for someone with muscular dystrophy
Muscular Dystrophy Campaign Trailblazers was created in 2008.
Muscular Dystrophy Family Foundation was created in 1958.
Genetic counseling is advised when there is a family history of muscular dystrophy. Women may have no symptoms but still carry the gene for the disorder. Duchenne muscular dystrophy can be detected with about 95% accuracy by genetic studies performed during pregnancy. http://www.nlm.nih.gov/medlineplus/ency/article/001190.htm http://en.wikipedia.org/wiki/Muscular_dystrophy
Muscular dystrophy is a group of genetic disorders that lead to progressive weakness and loss of muscle mass. This can result in difficulty with movement, breathing, and other physical functions. The severity of symptoms and progression of the disease can vary depending on the specific type of muscular dystrophy.