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glycogen storage disease |
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glycogen storage diseaseor glycogenosisAny of numerous types of hereditary enzyme deficiency resulting in altered metabolism of glycogen. The problems are classified in two groups, those affecting the liver and those involving striated muscle, both primary glycogen storage sites. Symptoms in the liver group range from symptomatic hypoglycemia with ketosis to asymptomatic liver enlargement (hepatomegaly). In the muscle group, they range from weakness and cramps to fatal heart enlargement. glycogen storage disease [′glī·kə·jən ′stȯr·ij di‚zēz] (medicine) How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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Myringostapediopexy, a term popularized by Juers, (1) is also known as a type III tympanoplasty in the Wullstein classification. SMA type III patients are able to walk, but weakness is prevalent. We found a shift from type IV to type III SCCmec element during 1992-2003, perhaps caused by selective pressure from indiscriminate use of antimicrobial drugs. |
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