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Case Reports
. 1978;83(1):65-70.
doi: 10.3109/03009737809179114.

Primary hyperoxaluria (glycolic acid variant): a clinical and genetical investigation of eight cases

G Holmgren, T Hörnström, S Johansson, G Samuelson
Case Reports

Primary hyperoxaluria (glycolic acid variant): a clinical and genetical investigation of eight cases

G Holmgren et al. Ups J Med Sci. 1978.

Abstract

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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