Primary Hyperoxaluria
1961; American College of Physicians; Volume: 55; Issue: 1 Linguagem: Inglês
10.7326/0003-4819-55-1-70
ISSN1539-3704
Autores Tópico(s)Biomedical Research and Pathophysiology
ResumoArticle1 July 1961Primary HyperoxaluriaANGUS W. MCLAURIN, WILLIAM R. BEISEL, GERALD J. MCCORMICK, M.S., RAYMOND SCALETTAR, ROBERT H. HERMANANGUS W. MCLAURIN, WILLIAM R. BEISEL, GERALD J. MCCORMICK, M.S., RAYMOND SCALETTAR, ROBERT H. HERMANAuthor, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-55-1-70 SectionsAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail ExcerptPrimary hyperoxaluria is characterized by an increased urinary excretion of oxalate and the deposition of calcium oxalate crystals in the kidneys and other organs. This metabolic defect was thought initially to be a severe disease of infancy and childhood, characterized by recurrent nephrolithiasis and pyelonephritis and by a progressive course terminating in a uremic death. Studies by Newns and Black (1) in 1953 and by Aponte and Fetter (2) in 1954 demonstrated an increased urinary excretion of oxalate prior to death in such patients. Subsequently, the disease has been diagnosed with increasing frequency during life, and others (3-7) have confirmed...References1. NEWNSBLACK GHJA: A case of calcium oxalate nephrocalcinosis. Great Ormond St. J., p. 40, 1953. Google Scholar2. APONTEFETTER GETR: Familial idiopathic oxalate nephrocalcinosis. Amer. J. Clin. Path. 24: 1363, 1954. CrossrefMedlineGoogle Scholar3. GODWINFOWLERDEMPSEYHENNEMAN JTMFEFPH: Primary hyperoxaluria and oxalosis: report of a case and review of the literature. New Engl. J. Med. 259: 1099, 1958. CrossrefMedlineGoogle Scholar4. PYRAHANDERSONHODGKINSONZAREMBSKI LNCKAPM: A case of oxalate nephrocalcinosis and primary hyperoxaluria. Brit. J. Urol. 31: 235, 1959. CrossrefMedlineGoogle Scholar5. SCOWENSTANSFELDWATTS EGAGRW: Oxalosis and primary hyperoxaluria. J. Path. Bact. 77: 195, 1959. 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