A case of hereditary angioedema which mimics the Familial Mediterranean Fever

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dc.authorscopusid55980458400
dc.authorscopusid57203921928
dc.authorscopusid37068136000
dc.authorscopusid55979665600
dc.authorscopusid50161113600
dc.contributor.authorAşcio?lu S.
dc.contributor.authorÇatal F.
dc.contributor.authorTopal E.
dc.contributor.authorErmiştekin H.
dc.contributor.authorErge D.
dc.date.accessioned2024-08-04T20:00:56Z
dc.date.available2024-08-04T20:00:56Z
dc.date.issued2013
dc.departmentİnönü Üniversitesien_US
dc.description.abstractHereditary angioedema is due to deficiency of C1 esterase inhibitor, inherited as an autosomal dominant trait, manifested by recurrent attacks of swelling of the face, trunk, extremities, airway and abdominal viscera. The disease may present with isolated abdominal pain and differential diagnosis should be done with Familial Mediterranean Fever. Our case, 8 years-old-female patient who was admitted with complaint of abdominal pain and vomiting. In history, patients had recurrent abdominal pain and vomiting since her 5th birthday and she was diagnosed with Familial Mediterranean Fever. She was treated with colchicine but had no release from the complaint. Differential diagnosis were done due to patients complaint were not associated with fever, elevated acute phase reactants and had family history of hereditary angioedema (patient's father had diagnosed with hereditary angioedema). Patient was screened for serum C4 and C1 inhibitory level. Diagnosis of hereditary angioedema was confirmed because of low level of C4 and C1 inhibitory concentration. Copyright © 2013 by Türki ye Klinikleri.en_US
dc.identifier.endpage199en_US
dc.identifier.issn1300-0381
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-84891470606en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage197en_US
dc.identifier.urihttps://hdl.handle.net/11616/91124
dc.identifier.volume22en_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.relation.ispartofTurkiye Klinikleri Pediatrien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAngioedemas, hereditaryen_US
dc.subjectFamilial Mediterranean Feveren_US
dc.titleA case of hereditary angioedema which mimics the Familial Mediterranean Feveren_US
dc.title.alternativeAilevi Akdeniz Ateşini taklit eden bir herediter anjiyoödem olgusuen_US
dc.typeArticleen_US

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