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Article

Idiopathic renal hypouricemia: A case report and literature review.

Molecular medicine reports - 1 Dec 2019

Wang Cuiyu, Wang Jin, Liu Song, Liang Xinhua, Song Yifan, Feng Ling, Zhong Lanxin, Guo Xiaohua

Abstract excerpt

Idiopathic renal hypouricemia is a rare hereditary condition. Type 2 renal hyperuricemia (RHUC2) is caused by a mutation in the SLC2A9 gene, which encodes a high‑capacity glucose and urate transporter, glucose transporter (GLUT)9. RHUC2 predisposes to exercise‑induced acute renal failure (EIARF) and nephrolithiasis, which is caused by a defect in renal tubular urate transport and is characterized by increased...

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Identifiers

PMID: 31638209
DOI: 10.3892/mmr.2019.10726
PMCID: PMC6854582

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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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