Primary hyperoxaluria diagnosed after kidney transplantation: a case report and literature review

BACKGROUND: Primary hyperoxaluria (PH) is a rare inherited autosomal recessive disease caused by disturbed glyoxylate metabolism. The disease is characterized by calcium oxalate crystal deposition in various organs, especially in the kidney. Due to the lack of current understanding of PH, nearly all...

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Detalles Bibliográficos
Autores principales: Cai, Zhitao, Ding, Mao, Chen, Rengui, Zhu, Jiefu, Li, Lian, Wu, Xiongfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626922/
https://www.ncbi.nlm.nih.gov/pubmed/34837989
http://dx.doi.org/10.1186/s12882-021-02546-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8626922/
https://www.ncbi.nlm.nih.gov/pubmed/34837989
http://dx.doi.org/10.1186/s12882-021-02546-0

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