A Rare Cause of Neonatal Liver Failure: Neonatal Hemochromatosis

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dc.contributor.authorUluca, Unal
dc.contributor.authorSivash, Ercan
dc.contributor.authorErkan, Melih Engin
dc.contributor.authorKervancioglu, Selim
dc.contributor.authorKarakok, Metin
dc.contributor.authorTan, Ilhan
dc.date.accessioned2024-04-24T17:47:54Z
dc.date.available2024-04-24T17:47:54Z
dc.date.issued2013
dc.departmentDicle Üniversitesien_US
dc.description.abstractNeonatal hemochromatosis (NH) is a severe rare liver disease in neonatal period associated with ekstrahepatic siderosis. This disease is characterized by hepatocellular insufficiency that presented with jaundice, hypoglycemia, hypoalbuminemia, low fibrinogen levels, thrombocytopenia, anemia, direct and indirect hyperbilirubinemia from the first days of life. Herein we reported a case with Rh incompatibility whose jaundice was noted at the first day of life and referred to our hospital for exchange transfusion, but thereafter diagnosed as NH and reviewed the literature in the view point of the latest developments related to the topic.en_US
dc.identifier.endpage47en_US
dc.identifier.issn1309-3878
dc.identifier.issue3en_US
dc.identifier.startpage44en_US
dc.identifier.urihttps://hdl.handle.net/11468/22801
dc.identifier.volume5en_US
dc.identifier.wosWOS:000420972400010
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.language.isotren_US
dc.publisherDuzce Univen_US
dc.relation.ispartofKonuralp Tip Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectNeonatal Hemochromatosisen_US
dc.subjectJaundiceen_US
dc.subjectRh Incompatibilityen_US
dc.titleA Rare Cause of Neonatal Liver Failure: Neonatal Hemochromatosisen_US
dc.titleA Rare Cause of Neonatal Liver Failure: Neonatal Hemochromatosis
dc.typeArticleen_US

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