dc.contributor.author | Shabestari, MS | |
dc.contributor.author | Rezaei, N | |
dc.date.accessioned | 2018-08-26T08:28:23Z | |
dc.date.available | 2018-08-26T08:28:23Z | |
dc.date.issued | 2008 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51493 | |
dc.description.abstract | BTK 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.iso | English | |
dc.relation.ispartof | JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY | |
dc.subject | allergy | |
dc.subject | asthma | |
dc.subject | BTK | |
dc.subject | X-linked agammaglobulinemia | |
dc.title | Asthma and allergic rhinitis in a patient with BTK deficiency | |
dc.type | Article | |
dc.citation.volume | 18 | |
dc.citation.issue | 4 | |
dc.citation.spage | 300 | |
dc.citation.epage | 304 | |
dc.citation.index | Web of science | |
dc.citation.URL | http://www.jiaci.org/issues/vol18issue4/11.pdf | |