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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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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

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