Alkaptonuria: Case report [Alkaptonüri]

dc.contributor.authorAkyürek, Fatma Tunçez
dc.contributor.authorBilgiç, Ö.
dc.contributor.authorKurtipek, Gülcan Saylam
dc.contributor.authorGezer, İlknur Albayrak
dc.contributor.authorAltınyazar, Hilmi Cevdet
dc.date.accessioned2020-03-26T19:08:00Z
dc.date.available2020-03-26T19:08:00Z
dc.date.issued2015
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractAlkaptonuria is a rare autosomal recessive condition arising as a result of a genetic deficiency of the enzyme homogentisic acid oxidase which has a role in the metabolism of tyrosine and phenylalanine. Blue-black discoloration which developes from excessive accumulation of homogentisic acid in various tissues such as connective tissue and cartilage due to deficiency of homogentisic acid oxidase enzyme, called ochronosis. The most important causes of morbidity are ochronotic arthropathy and cardiovascular involvement seen in fourth and sixth decades. There is no definitive treatment and treatment options generally are intended to prevent complications. Herein we report a 66-year-old woman diagnosed with alkaptonuria who presented with blue discoloration in auricle and nails. Alkaptonuria is a progressive systemic disease and it should be considered in the presence of appropriate clinical findings. © 2015 by Türkiye Klinikleri.en_US
dc.identifier.doi10.5336/dermato.2014-42697en_US
dc.identifier.endpage107en_US
dc.identifier.issn1300-0330en_US
dc.identifier.issue3en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage103en_US
dc.identifier.urihttps://dx.doi.org/10.5336/dermato.2014-42697
dc.identifier.urihttps://hdl.handle.net/20.500.12395/32757
dc.identifier.volume25en_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.publisherTurkiye Kliniklerien_US
dc.relation.ispartofTurkiye Klinikleri Dermatolojien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectAlkaptonuriaen_US
dc.subjectOchronosisen_US
dc.titleAlkaptonuria: Case report [Alkaptonüri]en_US
dc.typeArticleen_US

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