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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書誌詳細
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: BMC 2019-06-01
シリーズ:BMC Nephrology
主題:
Primary hyperoxaluria
Kidney transplantation failure
Calcium oxalate crystals
Case report
オンライン･アクセス:http://link.springer.com/article/10.1186/s12882-019-1402-2
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