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

Abstract 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 neph...

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Dades bibliogràfiques
Autors principals: Ruiming Cai, Minzhuang Lin, Zhiyong Chen, Yongtong Lai, Xianen Huang, Guozhi Zhao, Xuekun Guo, Zhongtang Xiong, Juan Chen, Hui Chen, Qingping Jiang, Shaoyan Liu, Yuexin Yang, Weixiang Liang, Minhui Zou, Tao Liu, Wenfang Chen, Hongzhou Liu, Juan Peng
Format: Artigo
Idioma:Inglês
Publicat: BMC 2019-06-01
Col·lecció:BMC Nephrology
Matèries:
Primary hyperoxaluria
Kidney transplantation failure
Calcium oxalate crystals
Case report
Accés en línia:http://link.springer.com/article/10.1186/s12882-019-1402-2
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