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dc.contributor.authorShabestari, MS
dc.contributor.authorRezaei, N
dc.date.accessioned2018-08-26T08:28:23Z
dc.date.available2018-08-26T08:28:23Z
dc.date.issued2008
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51493
dc.description.abstractBTK deficiency is a primary immunodeficiency disease characterized by the absence of circulating B cells and agammaglobulinemia. While recurrent bacterial infections are the most common manifestations, symptoms of allergy and asthma are rare. We present the case of a 7-year-old boy who presented with asthma symptoms, allergic rhinitis, and severe papular urticaria. He had a positive skin prick test to aeroallergens and food allergens. However, further laboratory tests revealed a low number of B cells and decreased serum levels of all immunoglobulin isotypes. Molecular analysis revealed a mutation in the BTK gene. Although patients with BTK deficiency seem to be protected from atopy, our patient had allergic symptoms suggesting a bias toward a type 2 helper T cell pattern in this case. Primary antibody deficiency should be considered in the differential diagnosis of pediatric allergy and asthma when respiratory infection persists despite appropriate treatment.
dc.language.isoEnglish
dc.relation.ispartofJOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY
dc.subjectallergy
dc.subjectasthma
dc.subjectBTK
dc.subjectX-linked agammaglobulinemia
dc.titleAsthma and allergic rhinitis in a patient with BTK deficiency
dc.typeArticle
dc.citation.volume18
dc.citation.issue4
dc.citation.spage300
dc.citation.epage304
dc.citation.indexWeb of science
dc.citation.URLhttp://www.jiaci.org/issues/vol18issue4/11.pdf


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