Gout and Glycogen Storage Disease

Article1 April 1963Gout and Glycogen Storage DiseaseH. EDWARD HOLLING, M.D., F.R.C.P.H. EDWARD HOLLING, M.D., F.R.C.P.Search for more papers by this authorAuthor, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-58-4-654 SectionsAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail ExcerptThis report completes the clinical account of a brother and 2 sisters who now have been reported 3 times, each time under a different diagnosis. They were first described in 1926 by Poynton and Wyllie (1) as examples of familial cirrhosis. This diagnosis was corrected in 1936 when they were again described in an account of glycogen storage disease of the liver by Ellis and Payne (2). Two of them are now presented as examples of gout associated with glycogen storage disease.All 3 patients appear to have had the form of glycogen storage disease in which the glucose-6-phosphatase activity...References1. 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Cori on the occasion of his seventieth birthday.: Types I, III, IV, V, VII and Unclassified GlycogenosesStudies of uric acid metabolism in glycogen storage disease associated with gouty arthritisRelationships between glycogen storage disease and tophaceous goutLaboratory Diagnosis of Glycogen DiseasesHyperuricemia in Primary and Renal HypertensionUric Acid Metabolism in Normal Man and in Primary GoutThe interrelationship of glycogen storage disease and goutGoutSignificance of the renal clearance of uric acid in normal and gouty manThe metabolism of a-keto acids in von Gierke's diseaseA Report on Two Adult Patients with Glycogen Storage Disease 1 April 1963Volume 58, Issue 4Page: 654-663KeywordsAcidsBlood plasmaCirrhosisGlycogen storage diseasesGoutLiverLiver diseasesPhotographyPlasma proteinsVascular medicine ePublished: 1 December 2008 Issue Published: 1 April 1963 PDF downloadLoading ...