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glycogen storage disease |
Also found in: Dictionary/thesaurus, Medical, Legal, Wikipedia, Hutchinson | 0.06 sec. |
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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P1 Type is the successor to the P Type IB Series precision planetary gear speed reducers developed for servomotors and launched in 2001. This scenario suggests that type Ib actually has more in common with type 11 supernovas than with type I. |
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