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PRIMARY HYPEROXALURIA
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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.
American Academy of Pediatrics (AAP)
Title: PRIMARY HYPEROXALURIA
Description:
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.
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PRIMARY HYPEROXALURIA
PRIMARY HYPEROXALURIA
Dietary and metabolic studies carried out on a patient with primary hyperoxaluria are reported. There was no appreciable change in the urinary excretion of oxalate when he was give...
PRIMARY HYPEROXALURIA
PRIMARY HYPEROXALURIA
The clinical and pathologic findings in a case of primary hyperoxaluria and calcium oxalate nephrocalcinosis in a 7-year-old boy are described and discussed in relation to similar ...
Response to Dietary Oxalate after Bariatric Surgery
Response to Dietary Oxalate after Bariatric Surgery
SummaryBackground and objectivesBariatric surgery (BS) may be associated with increased oxalate excretion and a higher risk of nephrolithiasis. This study aimed to investigate urin...