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Article

A molecular journey on the pathogenesis of primary hyperoxaluria.

Current opinion in nephrology and hypertension - 1 Jul 2024

Cellini Barbara

Abstract excerpt

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...

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Identifiers

PMID: 38602143
DOI: 10.1097/MNH.0000000000000987
PMCID: PMC11139248

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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