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Muscular dystrophy queensland was formed to assist the people of queensland living with muscular dystrophy and other neuromuscular disorders muscular dystrophy is a neuromuscular, genetic disorder which results in the progressive deterioration of muscle strength and function. Researchers and doctors are learning more about the causes of muscular dystrophy and various treatments are being trialled to stop the progression of the disease. It is estimated that there are more than 20, 000 people in australia who have some form of neuromuscular disease. The incidence of persons with a neuromuscular disorder is estimated to be 100 per 100, 000 head of population. While most forms of muscular dystrophy occur in babies or children, some others appear in late adolescence or adulthood. There are many other types of neuromuscular disorders, affecting people of all ages. Life expectancy for this disorder is usually only until early adulthood. The most common form in childhood is duchenne muscular dystrophy, which can see a young boy using a manual wheelchair by the age of 8, and being completely dependent on an electric one by his early teens. Nonetheless, through early diagnosis, proper therapy and support an increased quality of life is possible.
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