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Description of the Infection Duchenne muscular dystrophy is a genetic disorder that's characterized by progressive muscle degeneration and weakness. It's caused by a mutation of the DMD gene which could be inherited through transmission of an X-linked recessive gene. DMD codes to the muscle protein, dystrophin. As a result, those who are experiencing this disease are not able to make this protein in their muscles, making them become weak and never operate properly (NHGRI, 2014). This disease moves quickly throughout the human body and rapidly gets worse. Of the nine distinct muscular disorders, Duchenne muscular dystrophy is the most widespread form found in humans today (MDA, 2014). Epidemiology Duchenne muscle dystrophy affects approximately 1 in every 3,500 live male births; which is almost 20,000 new cases annually. This disease primarily affects young boys due to their disorderвЂ™s location to the вЂњXвЂќ chromosome. In very rare instances it affects young girls. The majority of the time, it simply makes them become carriers of the disease and they never show any signs. Duchenne muscular dystrophy isn't confined to only 1 race or culture; it affects all races and cultures. Typically, Duchenne muscular dystrophy can be passed down by an affected parent to their child; however, that is not necessarily true in every circumstance. Approximately 35 percent of children affected with the disease don't get it from their parents. This is possible since the disorder can occur in any child when there is mutation about the вЂњXвЂќ chromosome where DMD is located. This means that anyone may be affected by this disease even if it does not operate in their own family (PPMD, 2014). Tired of Inheritance A majority of people diagnosed with Duchenne muscular.