Duchenne muscular dystrophy is one of the nine types of muscular dystrophy and is more prominent in males than females. Duchenne MD is one of the most rapidly worsening types of muscular dystrophy and is caused by a defect in a particular muscle protein. Symptoms appear before the age of six and can be detected during infancy (A. D. A. M, 2012).
You have indicators of muscular dystrophy. You own a family or personal history of muscular dystrophy, and you and your partner are planning to bare children. Prevention. Generally, genetic counseling is highly advised when there are family antiquities of muscular dystrophy.
Essay on Duchenne Muscular Dystrophy. parents as they find out that their child has a form of muscular dystrophy. This particular type of muscular dystrophy is referred to as Duchenne Muscular Dystrophy, which is a genetically inherited disorder that is the most common and severe of all muscular dystrophies.
Duchenne’s Muscular Dystrophy Introduction: According to Wu, Kuban, Allred, Shapiro, and Darras, (2005), “Duchenne muscular dystrophy is an X-linkedrecessive degenerative neuromuscular disorder characterized by deficient dystrophin protein in muscle”. The rate of prevalence of Duchenne’s muscular dystrophy (DMD) is one in every thirty-five thousand males.
Duchenne Muscular Dystrophy is an inherited muscle weakening disease. Living with Duchenne Muscular Dystrophy is challenging and makes everyday life a struggle not only for the person living with it but for the family as well. There is currently no cure for DMD but luckily there is some hope. DMD affects individuals both physically and emotionally.
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Muscular Dystrophy Association Clinics. These clinics are located throughout the country and have specialists that diagnose and treat diseases like Duchenne. Learn more about the MDA; Parent Project Muscular Dystrophy (PPMD).