PRIMARY HYPEROXALURIA

1 May 1960

journal article
Published by American Academy of Pediatrics (AAP)

Vol. 25 (5) , 869-871
https://doi.org/10.1542/peds.25.5.869

Abstract

Hyperoxaluria has been studied in a family and found to be inherited as a probable autosomal dominant. Only one member of the family developed nephrocalcinosis. The possible existence of a second form of hyperoxaluria with elevated concentrations of uric acid in the blood is discussed.

Keywords

HYPEROXALURIA HYPEROXALURIA
MEMBER
INHERITED
PRIMARY HYPEROXALURIA
FAMILY DEVELOPED
PROBABLE AUTOSOMAL
DEVELOPED NEPHROCALCINOSIS

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