Primary hyperoxaluria diagnosed after kidney transplantation failure: lesson from 3 case reports and literature review

BACKGROUND: Primary hyperoxaluria (PH) is a rare inborn disorder of the metabolism of glyoxylate, which causes the hallmark production oxalate and forms insoluble calcium oxalate crystals that accumulate in the kidney and other organs. Since the manifestation of PH varies from recurrent nephrolithia...

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Detalles Bibliográficos
Autores principales: Cai, Ruiming, Lin, Minzhuang, Chen, Zhiyong, Lai, Yongtong, Huang, Xianen, Zhao, Guozhi, Guo, Xuekun, Xiong, Zhongtang, Chen, Juan, Chen, Hui, Jiang, Qingping, Liu, Shaoyan, Yang, Yuexin, Liang, Weixiang, Zou, Minhui, Liu, Tao, Chen, Wenfang, Liu, Hongzhou, Peng, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582561/
https://www.ncbi.nlm.nih.gov/pubmed/31215412
http://dx.doi.org/10.1186/s12882-019-1402-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582561/
https://www.ncbi.nlm.nih.gov/pubmed/31215412
http://dx.doi.org/10.1186/s12882-019-1402-2

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