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Article

Clinical features and mutational spectrum of Chinese patients with primary hyperoxaluria type 2.

Urolithiasis - 10 May 2024

Liu Yukun, Zhao Zhenqiang, Ge Yucheng, He Longzhi, Qi Siyu, Wang Wenying

Abstract excerpt

Primary hyperoxaluria type 2 (PH2) is a rare hereditary disease that causes nephrolithiasis, nephrocalcinosis and kidney failure. This study aimed to investigate the clinical features and mutational spectrum of Chinese patients with PH2. A retrospective cohort study was performed on PH2 patients admitted to our center over seven years. We also systematically reviewed all the articles on Chinese PH2 patients...

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PMID: 38727838
DOI: 10.1007/s00240-024-01579-y

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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