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2, 8 Dihydroxyadenine urolithiasis: A case report and review of literature
Adenine phosphoribosyl transferase deficiency is a rare metabolic abnormality presenting with 2,8 dihydroxyadenine urolithiasis. The stones are characteristically radiolucent and therefore need to be differentiated from uric acid stones which are also radiolucent and have identical chemical reactivi...
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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845193/ https://www.ncbi.nlm.nih.gov/pubmed/20352011 http://dx.doi.org/10.4103/0971-4065.50680 |
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author | Sreejith, P. Narasimhan, K. L. Sakhuja, V. |
author_facet | Sreejith, P. Narasimhan, K. L. Sakhuja, V. |
author_sort | Sreejith, P. |
collection | PubMed |
description | Adenine phosphoribosyl transferase deficiency is a rare metabolic abnormality presenting with 2,8 dihydroxyadenine urolithiasis. The stones are characteristically radiolucent and therefore need to be differentiated from uric acid stones which are also radiolucent and have identical chemical reactivity. No cases of 2, 8- dihydroxyadenine urolithiasis have been reported from India. We report a 3 year old child with 2, 8- dihydroxyadenine urolithiasis and acute renal failure. |
format | Text |
id | pubmed-2845193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-28451932010-03-26 2, 8 Dihydroxyadenine urolithiasis: A case report and review of literature Sreejith, P. Narasimhan, K. L. Sakhuja, V. Indian J Nephrol Case Report Adenine phosphoribosyl transferase deficiency is a rare metabolic abnormality presenting with 2,8 dihydroxyadenine urolithiasis. The stones are characteristically radiolucent and therefore need to be differentiated from uric acid stones which are also radiolucent and have identical chemical reactivity. No cases of 2, 8- dihydroxyadenine urolithiasis have been reported from India. We report a 3 year old child with 2, 8- dihydroxyadenine urolithiasis and acute renal failure. Medknow Publications 2009-01 /pmc/articles/PMC2845193/ /pubmed/20352011 http://dx.doi.org/10.4103/0971-4065.50680 Text en © Indian Journal of Nephrology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Sreejith, P. Narasimhan, K. L. Sakhuja, V. 2, 8 Dihydroxyadenine urolithiasis: A case report and review of literature |
title | 2, 8 Dihydroxyadenine urolithiasis: A case report and review of literature |
title_full | 2, 8 Dihydroxyadenine urolithiasis: A case report and review of literature |
title_fullStr | 2, 8 Dihydroxyadenine urolithiasis: A case report and review of literature |
title_full_unstemmed | 2, 8 Dihydroxyadenine urolithiasis: A case report and review of literature |
title_short | 2, 8 Dihydroxyadenine urolithiasis: A case report and review of literature |
title_sort | 2, 8 dihydroxyadenine urolithiasis: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845193/ https://www.ncbi.nlm.nih.gov/pubmed/20352011 http://dx.doi.org/10.4103/0971-4065.50680 |
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