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Primary Hyperoxaluria (Glycolic Acid Variant)
Author(s) -
Gösta Holmgren,
Thomas Hörnström,
Sven Erik Johansson,
Gösta Samuelson
Publication year - 1978
Publication title -
upsala journal of medical sciences
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.808
H-Index - 41
eISSN - 2000-1967
pISSN - 0300-9734
DOI - 10.3109/03009737809179114
Subject(s) - medicine , primary hyperoxaluria , nephrocalcinosis , glycolic acid , pyridoxine , transplantation , gastroenterology , kidney , lactic acid , biology , bacteria , genetics
The clinical features of eight cases of primary hyperoxaluria have been summarized. The possibility of different phenotypes is discussed. A reduction, but no normalization, of the oxalate formation during pyridoxine therapy was found. A renal transplantation performed in one of the patients failed because of the formation of nephrocalcinosis.

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