2024
DOI: 10.1097/mnh.0000000000000987
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A molecular journey on the pathogenesis of primary hyperoxaluria

Barbara Cellini

Abstract: Purpose of review Primary hyperoxalurias (PHs) are rare disorders caused by the deficit of liver enzymes involved in glyoxylate metabolism. Their main hallmark is the increased excretion of oxalate leading to the deposition of calcium oxalate stones in the urinary tract. This review describes the molecular aspects of PHs and their relevance for the clinical management of patients. Recent findings Recently, the study of PHs pathogenesis has received grea… Show more

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