Second transplantation after kidney graft loss in primary hyperoxaluria type 2: a pedigree study and mutation analysis

Second transplantation after kidney graft loss in primary hyperoxaluria type 2: a pedigree study and mutation analysis

Background Primary hyperoxaluria type 2 (PH2) is a rare disorder caused by GRHPR mutations. Research on the mutation spectrum and pedigree of PH2 helps in comprehending its pathogenesis and clinical outcomes, guiding clinical diagnosis and treatment.Methods We report a case of PH2 with a three-gener...

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Main Authors: Yushi Peng, Yingchun Zheng, Fu Xiong, Mingming Zhang, Yuchen Wang, Jia Luo, Wenli Zeng, Jialiang Hui, Wenfeng Deng, Jian Xu, Yun Miao, Renfei Xia, Yiling Fang
Format: Article
Language:English
Published: Taylor & Francis Group 2024-12-01
Series:Renal Failure
Subjects:
primary hyperoxaluria type 2
GRHPR
kidney transplantation
pedigree
mutation
functional analysis
Online Access:https://www.tandfonline.com/doi/10.1080/0886022X.2024.2417743
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https://www.tandfonline.com/doi/10.1080/0886022X.2024.2417743

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