Paper Summary:

The paper begins with describing the disease and examines its symptoms and forms. It then looks at ways to diagnose the disease through EMGs nerve conduction velocity, muscle biopsy, blood enzyme testing and other genetic testing. The question of treatment is then discussed , specifying treatment such as multidisciplinary team care, adaptive equipment, exercise, diet, orthopedics, surgery, medication, respiratory therapy, and counseling. Current research of the disease is discussed, concluding with a brief history of muscular dystrophy research.

From the Paper:

"Muscular dystrophy is a crippling disorder caused by the gradual wasting of skeletal muscle and is the most common muscle disease of children. Its course is progressive, with increased weakness and reduction of muscle mass and function. This is caused by changes in the physical and chemical structure of the surface and the internal membranes of the muscle cells. In addition, these children may have learning disabilities or cognitive impairments (Batshaw, 1997). Although the chromosomal location and the underlying gene for most forms of muscular dystrophy have been identified, remission does not occur (Case-Smith, 2001). Clinical forms of the disease are recognized based on the pattern of inheritance, age when symptoms are first noticed, and distribution of the muscles earliest involved."

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