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

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.
Authors	G Holmgren, T Hörnström, S Johansson, G Samuelson
Journal	Upsala journal of medical sciences (Ups J Med Sci) Vol. 83 Issue 1 Pg. 65-70 ( 1978) ISSN: 0300-9734 [Print] Sweden
PMID	705974 (Publication Type: Case Reports, Journal Article)
Chemical References	Glycolates Glyoxylates Oxalates
Topics	Adolescent Adult Child Child, Preschool Female Follow-Up Studies Glycolates (urine) Glyoxylates (urine) Humans Infant Kidney Calculi (genetics, urine) Male Middle Aged Nephrocalcinosis (genetics, urine) Oxalates (urine) Pedigree Uremia (genetics, urine) Ureteral Calculi (genetics, urine)

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