Anaesthesia recommendations for patients suffering from Alkaptonuria

dc.contributor.authorKastsiuchenka, Siarhei
dc.contributor.authorGerçek İrban, Arzu
dc.contributor.authorRanganath, Lakshminarayan
dc.contributor.authorDavidson, John
dc.date.accessioned2022-03-31T12:08:11Z
dc.date.available2022-03-31T12:08:11Z
dc.date.issued2014
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümü, Anesteziyoloji ve Reanimasyon Ana Bilim Dalı
dc.description.abstractAlkaptonuria (AKU) is a rare autosomal recessive disorder with an incidence of 1:250 000 to 1:1000 000 live births. AKU is caused by a deficiency of the enzyme homogentisate 1,2-dioxygenase (HGO). This enzyme converts homogentisic acid (HGA) to maleylacetoacetic acid in the tyrosine degradation pathway. Accumulated HGA is rapidly cleared in the kidney and excreted in the urine. HGA blood levels are kept very low through rapid kidney clearance, but over time HGA is deposited in cartilage throughout the body and converted to a pigment-like polymer. This occurs through an enzyme-mediated reaction in collagenous tissues like ligaments, tendons, cartilage, and sclera.
dc.identifier.citationKastsiuchenka, S., Gerçek İrban, A., Ranganath, L. ve Davidson, J. (2014). Anaesthesia recommendations for patients suffering from Alkaptonuria. Anästhesiologie & Intensivmedizin, 55(4).
dc.identifier.issn0170-5334
dc.identifier.issn1439-0256
dc.identifier.issue4
dc.identifier.urihttps://hdl.handle.net/20.500.12511/9188
dc.identifier.volume55
dc.identifier.wos000760384900002en_US
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.institutionauthorGerçek İrban, Arzu
dc.language.isoen
dc.publisherAktiv Druck & Verlag GmbH
dc.relation.ispartofAnästhesiologie & Intensivmedizinen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAlkaptonuria
dc.subjectPatients Suffering
dc.subjectAnaesthesia
dc.titleAnaesthesia recommendations for patients suffering from Alkaptonuria
dc.typeArticle

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