Abdominal pain due to hereditary angioedema: Case Report [Herediter anjiyoödeme ba?li karin a?risi]

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dc.contributor.authorTuran, Hakan
dc.contributor.authorBeşir, Fahri Halit
dc.contributor.authorBüyükkaya, Ramazan
dc.contributor.authorYaşar, Mehmet
dc.contributor.authorDoğan, Sami
dc.date.accessioned2020-04-30T13:32:05Z
dc.date.available2020-04-30T13:32:05Z
dc.date.issued2012
dc.departmentDÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.description.abstractHereditary angioedema is a disease characterized by subcutaneous edema without urticaria, upper airway obstruction, and gastrointestinal symptoms. It results from congenital deficiency of C1 esterase inhibitor. This rarely seen disease is autosomal dominant inherited, and severe forms can be life threatening. Here, we present a case of hereditary angioedema who applied to the emergency room with severe abdominal pain, with low levels of C1 esterase inhibitor and C4 and with specific ultrasound findings, and completely recovered with the application of C1 esterase inhibitor concentrate. Copyright © 2012 by Türkiye Klinikleri.en_US
dc.identifier.endpage106en_US
dc.identifier.issn1300-0330
dc.identifier.issue2en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage104en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12684/56
dc.identifier.volume22en_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.relation.ispartofTurkiye Klinikleri Dermatolojien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAbdominal pain; Angioedemas, hereditary; Complement C1 inhibitor proteinen_US
dc.titleAbdominal pain due to hereditary angioedema: Case Report [Herediter anjiyoödeme ba?li karin a?risi]en_US
dc.typeArticleen_US

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