Primary hyperoxaluria diagnosed after kidney transplantation: a case report and literature review
Abstract 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, ne...
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| Auteurs principaux: | , , , , , |
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| Format: | article |
| Langue: | EN |
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BMC
2021
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| Accès en ligne: | https://doaj.org/article/7ddbff7b95704f128e57a4187847511a |
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