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glycogen storage disease type viii		An x-linked recessive hepatic glycogen storage disease resulting from lack of expression of phosphorylase-b-kinase activity. Symptoms are relatively mild; hepatomegaly, increased liver glycogen, and decreased leukocyte phosphorylase are present. Liver shrinkage occurs in response to glucagon. [ Articles | Books | Images | Discussion groups ]
Additional comments : (Glycogenosis 8)

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