Outcomes of liver–kidney transplantation in patients with primary hyperoxaluria: an analysis of the scientific registry of transplant recipients database

Outcomes of liver–kidney transplantation in patients with primary hyperoxaluria: an analysis of the scientific registry of transplant recipients database

Abstract Background Primary hyperoxaluria (PH) is an inherited disease lacking of hepatic oxalic acid metabolic enzymes which could lead to irreverisible renal damage. Currently, liver–kidney transplantation is a curative but highly invasive therapy used to treat patients with PH. However, limited s...

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Bibliographic Details
Main Authors: Jie Xiang, Zheng Chen, Fangshen Xu, Shengmin Mei, Zhiwei Li, Jie Zhou, Yinlei Dong, Yangjun Gu, Zhichao Huang, Zhenhua Hu
Format: Article
Language:English
Published: BMC 2020-07-01
Series:BMC Gastroenterology
Subjects:
Primary hyperoxaluria
Inherited disease
Liver–kidney transplantation
Combined liver and kidney transplantation
Sequential liver and kidney transplantation
Online Access:http://link.springer.com/article/10.1186/s12876-020-01349-1

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http://link.springer.com/article/10.1186/s12876-020-01349-1

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