A brief history of the discovery and early treatment of this disease followed by an in depth analysis at the molecular level, ending with a summary of treatments and the future of research.
Written in 2001; 1,345 words; 5 sources; $ 45.95
Paper Summary:
This paper details the various issues and describes the research surrounding Duchenne's Muscular Dystrophy (DMD), a disease that affects children, primarily males and is characterized by the degeneration of muscular tissue. The essay discusses symptoms, causes, molecular and cellular defects, how symptoms are derived from cellular defects and possible treatments. The sections covering the molecular aspects of this disease are in depth and scientifically explicit.
From the Paper:
"Muscular Dystrophy is a debilitating disorder that is characterized by degeneration of muscle tissue. One of the most common forms of this disorder and one that is particularly severe is Duchenne's Muscular Dystrophy (DMD). This disease affects a far greater number of males, approximately 1 out of every 3 500 born, than females (Cooper 1997). The cellular defects associated with DMD are well understood; however, there is still some speculation over the actions that take place at the molecular level. The treatment available for DMD patients is very limited. However, there has been promising research done with stem cells, antibiotics and gene therapies that offer new hope for sufferers of DMD. Many of these studies have been done on mdx mice, an animal model for DMD that possesses the same genetic defect as humans who suffer with the disease (Agrawal et al. 1999). These studies offer a new ray of hope, not only for those suffering with DMD, but also for people who suffer from various types of muscular degenerative diseases."
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