| 2, 8 Dihydroxyadenine urolithiasis: A case report and review of literature. | |
| | |
MedLine Citation:
|
PMID: 20352011 Owner: NLM Status: In-Data-Review |
Abstract/OtherAbstract:
|
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. |
| | |
Authors:
|
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: - Revised Date: - |
Medline Journal Info:
|
Nlm Unique ID: 8914356 Medline TA: Indian J Nephrol Country: India |
Other Details:
|
Languages: eng Pagination: 34-6 Citation Subset: - |
Affiliation:
|
Department of Nephrology, PGIMER, Chandigarh, India. |
Export Citation:
|
APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
|
|
| Comments/Corrections | |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
Previous Document: Zygomycosis in a renal allograft recipient.
Next Document: Reinforcement Learning and Savings Behavior.