Primary hyperoxaluria type I diagnosed after a kidney transplant presenting with subcutaneous calcification: a case report of sodium thiosulfate treatment

Primary hyperoxaluria type I diagnosed after a kidney transplant presenting with subcutaneous calcification: a case report of sodium thiosulfate treatment

Primary hyperoxaluria (PH) is a rare autosomal recessive disorder that results from the overproduction of endogenous oxalate. The diagnosis of PH is often delayed or missed owing to its rarity, variable clinical expression and other diagnostic challenges. In this study, we report a patient with a fr...

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Bibliographic Details
Main Authors: Min Wu, Jing Lu, Yu-Jia Wang, Yong-Qi Li, Qing Wei, Yu-Xiang Gong, Ri-Ning Tang
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-05-01
Series:Frontiers in Pharmacology
Subjects:
primary hyperoxaluria
AGXT gene
subcutaneous calcification
skin biopsy
sodium thiosulfate
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2025.1485024/full
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https://www.frontiersin.org/articles/10.3389/fphar.2025.1485024/full

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