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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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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
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author Verma, Ritu
Niraimathi, Manickam
Prasad, Pallavi
Agrawal, Vinita
author_facet Verma, Ritu
Niraimathi, Manickam
Prasad, Pallavi
Agrawal, Vinita
author_sort Verma, Ritu
collection PubMed
description 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.
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spelling pubmed-61471972018-09-25 Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure Verma, Ritu Niraimathi, Manickam Prasad, Pallavi Agrawal, Vinita Kidney Res Clin Pract Case Report 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. Korean Society of Nephrology 2018-09 2018-09-30 /pmc/articles/PMC6147197/ /pubmed/30254853 http://dx.doi.org/10.23876/j.krcp.2018.37.3.287 Text en Copyright © 2018 by The Korean Society of Nephrology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Verma, Ritu
Niraimathi, Manickam
Prasad, Pallavi
Agrawal, Vinita
Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure
title Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure
title_full Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure
title_fullStr Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure
title_full_unstemmed Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure
title_short Dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure
title_sort dihydroxyadenine crystal-induced nephropathy presenting with rapidly progressive renal failure
topic Case Report
url 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
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