Delayed diagnosis of selective immunoglobulin deficiency: A case report

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dc.contributor.authorYilmaza, Ahmet
dc.contributor.authorEsmerb, Fatih
dc.contributor.authorKaradasc, Sevdegul
dc.contributor.authorKarsa, Veysel
dc.contributor.authorCelepkolua, Tahsin
dc.date.accessioned2024-04-24T19:07:45Z
dc.date.available2024-04-24T19:07:45Z
dc.date.issued2016
dc.departmentDicle Üniversitesien_US
dc.description.abstractArticle HistoryReceived Accepted 08 / 02 / 201603 / 04 / 2016Selective immunoglobulin A deficiency (SIgAD) is the most common of all primary immunodeficiency diseases; however, the pathogenesis has not been fully understood. Although most people with SIgAD are asymptomatic, some may present with recurrent infections; such as respiratory disorders, gastrointestinal tracts disorders, and allergic disorders. Herein, we report a case with SIgAD who presented with the complaints of pruritus, dental caries and chronic sinopulmonary infectionsen_US
dc.identifier.endpage65en_US
dc.identifier.issn1309-4483
dc.identifier.issn1309-5129
dc.identifier.issue3en_US
dc.identifier.startpage63en_US
dc.identifier.trdizinid259374
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/259374
dc.identifier.urihttps://hdl.handle.net/11468/27591
dc.identifier.volume33en_US
dc.indekslendigikaynakTR-Dizin
dc.language.isoenen_US
dc.relation.ispartofJournal of Experimental and Clinical Medicine
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleDelayed diagnosis of selective immunoglobulin deficiency: A case reporten_US
dc.titleDelayed diagnosis of selective immunoglobulin deficiency: A case report
dc.typeArticleen_US

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