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2, 8 Dihydroxyadenine urolithiasis: A case report and review of literature.
MedLine Citation:
PMID:  20352011     Owner:  NLM     Status:  PubMed-not-MEDLINE    
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.
P Sreejith; K L Narasimhan; V Sakhuja
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Indian journal of nephrology     Volume:  19     ISSN:  1998-3662     ISO Abbreviation:  Indian J Nephrol     Publication Date:  2009 Jan 
Date Detail:
Created Date:  2010-03-30     Completed Date:  2011-07-14     Revised Date:  2013-05-29    
Medline Journal Info:
Nlm Unique ID:  8914356     Medline TA:  Indian J Nephrol     Country:  India    
Other Details:
Languages:  eng     Pagination:  34-6     Citation Subset:  -    
Department of Nephrology, PGIMER, Chandigarh, India.
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