Effect of liver transplantation with primary hyperoxaluria type 1: Five case reports and review of literature

BACKGROUND: Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disease stemming from a deficiency in liver-specific alanine-glyoxylate aminotransferase, resulting in increased endogenous oxalate deposition and end-stage renal disease. Organ transplantation is the only effective treatme...

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Detalles Bibliográficos
Autores principales: Wang, Xin-Yue, Zeng, Zhi-Gui, Zhu, Zhi-Jun, Wei, Lin, Qu, Wei, Liu, Ying, Tan, Yu-Le, Wang, Jun, Zhang, Hai-Ming, Shi, Wen, Sun, Li-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979304/
https://www.ncbi.nlm.nih.gov/pubmed/36874433
http://dx.doi.org/10.12998/wjcc.v11.i5.1068

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979304/
https://www.ncbi.nlm.nih.gov/pubmed/36874433
http://dx.doi.org/10.12998/wjcc.v11.i5.1068

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