Document Detail


2,8-Dihydroxyadenine urolithiasis: report of an adult case in the United States.
MedLine Citation:
PMID:  3806829     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
2,8-Dihydroxyadeninuria is a rare purine metabolic disorder that has been reported to have caused urolithiasis in 14 cases, mostly children. Excretion of the hydroxylated metabolites of adenine results from a deficiency of adenine phosphoribosyltransferase. The insoluble calculi have a similar chemical structure to uric acid and frequently are misdiagnosed as uric acid calculi. Management differs from that of uric acid urolithiasis. We report on an adult with 2,8-dihydroxyadenine urolithiasis in the United States.
Authors:
M J Manyak; F J Frensilli; H C Miller
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Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  The Journal of urology     Volume:  137     ISSN:  0022-5347     ISO Abbreviation:  J. Urol.     Publication Date:  1987 Feb 
Date Detail:
Created Date:  1987-03-09     Completed Date:  1987-03-09     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0376374     Medline TA:  J Urol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  312-4     Citation Subset:  AIM; IM    
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MeSH Terms
Descriptor/Qualifier:
Adenine / analogs & derivatives*,  analysis
Adenine Phosphoribosyltransferase / deficiency*
Female
Humans
Middle Aged
Pentosyltransferases / deficiency*
Purine-Pyrimidine Metabolism, Inborn Errors / complications,  epidemiology*
United States
Urinary Calculi / analysis*,  etiology
Chemical
Reg. No./Substance:
30377-37-8/2,8-dihydroxyadenine; 73-24-5/Adenine; EC 2.4.2.-/Pentosyltransferases; EC 2.4.2.7/Adenine Phosphoribosyltransferase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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