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Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report

Primary hyperoxaluria type 2 is a rare autosomal recessive disorder caused by glyoxylate reductase/hydroxypyruvate reductase deficiency and characterized by recurrent episodes of nephrolithiasis and nephrocalcinosis. Herein, we describe a case of primary hyperoxaluria type 2 in a 33-year-old man who...

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Detalles Bibliográficos
Autores principales:	Liu, Si, Gao, Baoshan, Wang, Gang, Wang, Weigang, Lian, Xin, Wu, Shan, Yu, Jinyu, Fu, Yaowen, Zhou, Honglan
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2018
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840950/ https://www.ncbi.nlm.nih.gov/pubmed/29545831 http://dx.doi.org/10.3892/etm.2018.5841

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