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Rare crystalline nephropathy leading to acute graft dysfunction: a case report
BACKGROUND: Adenine phosphoribosyl transferase (APRT) deficiency is a rare genetic form of kidney stones and/or kidney failure characterized by intratubular precipitation of 2,8 dihydroxyadenine crystals. Early diagnosis and prompt management can completely reverse the kidney injury. CASE PRESENTATI...
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| 出版年: | BMC Nephrol |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6873418/ https://ncbi.nlm.nih.gov/pubmed/31752739 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-019-1616-3 |
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