Duchenne Muscular Dystrophy: Literature Review Research Paper.
Muscular Dystrophy's overview Introduction Since its discovery in 1860 by Guillaume Duchenne, Muscular Dystrophy (abbreviated MD) has become recognized as one of the most dangerous muscular disorders in the world (Duchenne Muscular Dystrophy, 1) Muscular Dystrophy is a serious muscular condition where the tissue weakens in the extremities.Also check our tips on how to write a research paper, see the lists of health research paper topics, and browse research paper examples. Introduction Muscular dystrophy (MD), as described by Walton and Nattrass in 1954, is a heterogeneous group of inherited primary diseases of the muscle, clinically characterized by progressive muscle weakness and wasting.Duchenne Muscular Dystrophy is an important genetic disorder to fully understand through the knowledge of research and information, due to the fact that it affects 1 in every 3,600 male births worldwide. The affects can vary between family, loved ones, and those who suffer with DMD.
Research In Duchenne muscular dystrophy (DMD), muscle is missing a key structural protein called dystrophin, making it more susceptible to injury. Eventually the body cannot keep up with repair and regeneration, which leads to muscle loss (wasting) and weakness.Myotonic dystrophy. As with other types of muscular dystrophy, myotonic dystrophy involves progressive muscle weakness and muscle wasting. However, it's often the smaller muscles that are affected first, such as those in the face, jaw and neck. Myotonic dystrophy can appear at any time between birth and old age.
The NIH is expanding and intensifying its research efforts on the muscular dystrophies and has established the Senator Paul D. Wellstone Muscular Dystrophy Cooperative Research Centers of Excellence to promote basic and clinical research on these disorders. Six Wellstone Centers are currently funded by NINDS, NIAMS, NICHD, and NHLBI.
