Pompe disease is an inherited disorder brought on by the buildup of a fancy sugar referred to as glycogen in the body's cells. The accumulation of glycogen in sure organs and tissues, especially muscles, impairs their skill to function normally. Researchers have described three varieties of Pompe disease, which differ in severity and Healthy Flow Blood health the age at which they appear. These varieties are known as traditional infantile-onset, non-basic infantile-onset, and Healthy Flow Blood late-onset. The traditional type of infantile-onset Pompe disease begins within a few months of start. Infants with this disorder sometimes experience muscle weakness (myopathy), poor muscle tone (hypotonia), an enlarged liver (hepatomegaly), and coronary heart defects. Affected infants may fail to realize weight and develop on the expected price (failure to thrive) and have breathing problems. If untreated, this type of Pompe disease results in death from coronary heart failure in the first 12 months of life. The non-traditional form of infantile-onset Pompe disease normally appears by age 1. It's characterized by delayed motor expertise (comparable to rolling over and sitting) and progressive muscle weakness.

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Ivy, John & Portman, Robert. Nutrient Timing: The way forward for Sports Nutrition. Aragon, Alan Albert