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Can Respir J ; 21(1): 17-9, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24288697

RESUMO

Severe combined immunodeficiency (SCID) is considered to be a pediatric emergency, with respiratory distress being the most common presenting symptom. The authors present two cases of SCID in children <4 months of age with respiratory distress at a tertiary care centre due to a recently described homozygous CD3 delta mutation found only in the Mexican Mennonite population. Failure to respond to broad-spectrum antibiotics prompted investigation for possible SCID. Bronchial alveolar lavage fluid from both patients grew Pneumocystis jiroveci, and flow cytometry revealed absent T cells. The CD3 delta gene is believed to be important in T cell differentiation and maturation. The present article reminds pediatricians and pediatric respirologists that the key to diagnosing SCID is to have a high index of suspicion if there is poor response to conventional therapies.


Assuntos
Complexo CD3/genética , Infecções Respiratórias/diagnóstico por imagem , Imunodeficiência Combinada Severa/diagnóstico , Canadá , Humanos , Lactente , Masculino , México/etnologia , Radiografia , Infecções Respiratórias/imunologia , Imunodeficiência Combinada Severa/genética , Imunodeficiência Combinada Severa/imunologia , Centros de Atenção Terciária
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