Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/5239
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dc.contributor.authorErgin, Hacer-
dc.contributor.authorBaşkan, Merve-
dc.contributor.authorAkalın, Necdet-
dc.contributor.authorGürses, Dolunay-
dc.date.accessioned2019-08-16T11:43:29Z
dc.date.available2019-08-16T11:43:29Z
dc.date.issued2003-
dc.identifier.issn0041-4301-
dc.identifier.urihttps://hdl.handle.net/11499/5239-
dc.description.abstractHereditary angioedema (HAE) results from a congenital deficiency of C1 inhibitor and is characterized by submucosal and subcutaneous edema of skin, larynx and abdomen. Occasional reports have appeared linking HAE with autoimmune diseases. We report a case of HAE presenting recurrent nondeforming polyarthritis, erythema marginatum-like rash and chest pain. There were no significant radiographic joint changes. Serologic tests for rheumatologic and autoimmune diseases were negative. After danazol treatment, physical examination and laboratory findings were normal over five years. We suggest that pediatricians should be aware of this rare disease and treat patients accordingly.en_US
dc.language.isoenen_US
dc.relation.ispartofTurkish Journal of Pediatricsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectC1 inhibitor deficiencyen_US
dc.subjectHereditary angioedemaen_US
dc.subjectadrenalinen_US
dc.subjectbenzathine penicillinen_US
dc.subjectcomplement component C1s inhibitoren_US
dc.subjectdanazolen_US
dc.subjectdiphenhydramineen_US
dc.subjectsalicylic aciden_US
dc.subjectsteroiden_US
dc.subjecttranexamic aciden_US
dc.subjectabdominal diseaseen_US
dc.subjectadolescenten_US
dc.subjectangioneurotic edemaen_US
dc.subjectarticleen_US
dc.subjectautoimmune diseaseen_US
dc.subjectcase reporten_US
dc.subjectchild careen_US
dc.subjectdiagnostic erroren_US
dc.subjectdisease associationen_US
dc.subjecterythemaen_US
dc.subjecthumanen_US
dc.subjectjoint radiographyen_US
dc.subjectlaboratory testen_US
dc.subjectlarynx edemaen_US
dc.subjectmaleen_US
dc.subjectmutational analysisen_US
dc.subjectpediatricianen_US
dc.subjectphysical examinationen_US
dc.subjectpolyarthritisen_US
dc.subjectpolymerase chain reactionen_US
dc.subjectprotein deficiencyen_US
dc.subjectrashen_US
dc.subjectrecurrent diseaseen_US
dc.subjectrestriction fragment length polymorphismen_US
dc.subjectrheumatic feveren_US
dc.subjectserologyen_US
dc.subjectskin edemaen_US
dc.subjectthorax painen_US
dc.subjecttreatment outcomeen_US
dc.subjectAdolescenten_US
dc.subjectAngioneurotic Edemaen_US
dc.subjectArthritisen_US
dc.subjectChest Painen_US
dc.subjectDanazolen_US
dc.subjectDiagnosis, Differentialen_US
dc.subjectErythemaen_US
dc.subjectEstrogen Antagonistsen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectRecurrenceen_US
dc.titleA case of hereditary angioedema with recurrent arthritis, erythema marginatum-like rash and chest painen_US
dc.typeArticleen_US
dc.identifier.volume45en_US
dc.identifier.issue3en_US
dc.identifier.startpage261
dc.identifier.startpage261en_US
dc.identifier.endpage264en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid14696809en_US
dc.identifier.scopus2-s2.0-0242523152en_US
dc.identifier.wosWOS:000187576000016en_US
dc.identifier.scopusqualityQ3-
dc.ownerPamukkale_University-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.openairetypeArticle-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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