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Artigo em Inglês | MEDLINE | ID: mdl-18714539

RESUMO

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.


Assuntos
Agamaglobulinemia/complicações , Asma/complicações , Proteínas Tirosina Quinases/deficiência , Rinite Alérgica Perene/complicações , Tirosina Quinase da Agamaglobulinemia , Agamaglobulinemia/imunologia , Asma/imunologia , Asma/metabolismo , Criança , Feminino , Humanos , Infecções/complicações , Infecções/imunologia , Masculino , Monócitos/enzimologia , Linhagem , Proteínas Tirosina Quinases/sangue , Rinite Alérgica Perene/imunologia
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