Alkaptonuria and intramedullary calcification.

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dc.contributor.authorRaina, Sen_US
dc.contributor.authorMahesh, D Men_US
dc.contributor.authorKaushal, S Sen_US
dc.contributor.authorGupta, Den_US
dc.contributor.authorDhiman, D Sen_US
dc.contributor.authorNegi, Aen_US
dc.contributor.authorSharma, Sen_US
dc.date.accessioned2008-07-14en_US
dc.date.accessioned2009-05-30T22:10:53Z
dc.date.available2008-07-14en_US
dc.date.available2009-05-30T22:10:53Z
dc.date.issued2008-07-14en_US
dc.description.abstractAlkaptonuria is a rare disorder of metabolism caused by deficiency of homogentisic acid oxidase enzyme and characterized by triad of homogentisic aciduria (dark urine), relentlessly progressive arthritis and ochronosis. We have documented a case with typical features of alkaptonuria along with intramedullary calcification which has not been reported in the literature before.en_US
dc.description.affiliationDepartment of Medicine, Indira Gandhi Medical College, Shimla.en_US
dc.identifier.citationRaina S, Mahesh DM, Kaushal SS, Gupta D, Dhiman DS, Negi A, Sharma S. Alkaptonuria and intramedullary calcification. Journal of the Association of Physicians of India. 2008 Jul; 56(): 552-5en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/89291
dc.language.isoengen_US
dc.source.urihttps://www.japi.orgen_US
dc.subject.meshAlkaptonuria --diagnosisen_US
dc.subject.meshCalcinosis --diagnosisen_US
dc.subject.meshDisease Progressionen_US
dc.subject.meshHomogentisate 1,2-Dioxygenaseen_US
dc.subject.meshHomogentisic Aciden_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle Ageden_US
dc.subject.meshOchronosis --physiopathologyen_US
dc.subject.meshRisk Factorsen_US
dc.titleAlkaptonuria and intramedullary calcification.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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