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Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure

Adenine phosphoribosyltransferase enzyme deficiency is a rare, autosomal recessive disorder. It is a disease limited to the renal system and usually presents with urolithiasis. Herein, we report a young female with dihydroxyadenine (DHA) crystal-induced nephropathy presenting with rapidly progressiv...

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Detalles Bibliográficos
Autores principales: Verma, Ritu, Niraimathi, Manickam, Prasad, Pallavi, Agrawal, Vinita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Nephrology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147197/
https://www.ncbi.nlm.nih.gov/pubmed/30254853
http://dx.doi.org/10.23876/j.krcp.2018.37.3.287
Descripción
Sumario:Adenine phosphoribosyltransferase enzyme deficiency is a rare, autosomal recessive disorder. It is a disease limited to the renal system and usually presents with urolithiasis. Herein, we report a young female with dihydroxyadenine (DHA) crystal-induced nephropathy presenting with rapidly progressive renal failure. DHA crystals can be easily diagnosed by their pathognomic color and shape in urine and biopsy specimens. A high index of clinical suspicion helps in the early diagnosis of this potentially treatable renal disease.