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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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| Publicado no: | BMC Nephrol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | 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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