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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Detalles Bibliográficos
Autores principales: Bagai, Sahil, Khullar, Dinesh, Bansal, Bhavna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873418/
https://www.ncbi.nlm.nih.gov/pubmed/31752739
http://dx.doi.org/10.1186/s12882-019-1616-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873418/
https://www.ncbi.nlm.nih.gov/pubmed/31752739
http://dx.doi.org/10.1186/s12882-019-1616-3

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