Different Pompe disease therapeutic options can help ease its symptoms. Enzyme replacement therapy (ERT) is an approved treatment for people with Pompe disease. Pompe disease is a genetic disorder that results from the deficiency of an enzyme called acid alfa glucosidase (GAA), which breaks down complex sugars in the body. Currently, the life expectancy for late-onset Pompe disease is estimated to be 30 years when it first appears in children or teenagers, and 50 years for adults. Without Pompe disease therapeutic, infants will die. Most of the people have, heart problems, respiratory (breathing) problems, and almost all are plagued with muscle weakness. Thus, they will have to use wheelchairs or oxygen at some point.
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