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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/42904
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dc.contributor.authorJoynt, G.-
dc.contributor.authorAbdullah, V.-
dc.contributor.authorWormald, P.-
dc.date.issued2001-
dc.identifier.citationEar, Nose and Throat Journal, 2001; 80(5):321-324-
dc.identifier.issn0145-5613-
dc.identifier.issn1942-7522-
dc.identifier.urihttp://hdl.handle.net/2440/42904-
dc.description.abstractHereditary angioedema is caused by an absolute deficiency or the functional inactivity of C1 esterase inhibitor in plasma. A precise diagnosis is important because, unlike allergic forms of mucocutaneous edema, this condition does not respond to epinephrine, antihistamines, or corticosteroids. We report the case of a 24-year-old man who experienced an acute attack after he had stopped taking his prophylactic medication.-
dc.language.isoen-
dc.publisherMedquest Communications, LLC-
dc.source.urihttp://findarticles.com/p/articles/mi_m0BUM/is_/ai_75577729-
dc.subjectNasal Septum-
dc.subjectTurbinates-
dc.subjectHumans-
dc.subjectAdolescent-
dc.subjectAdult-
dc.subjectAged-
dc.subjectMiddle Aged-
dc.titleHereditary angioedema: Report of a case-
dc.typeJournal article-
dc.identifier.doi10.1177/014556130108000509-
pubs.publication-statusPublished-
dc.identifier.orcidWormald, P. [0000-0001-7753-7277]-
Appears in Collections:Aurora harvest
Surgery publications

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