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Volume 35, Number 3, September 2002

DiGeorge sequence with hypogammaglobulinemia: a case report

Yin-Hsiu Chien, Yao-Hsu Yang, Shau-Yin Chu, Wuh-Liang Hwu, Pao-Lin Kuo, Bor-Luen Chiang
Department of Pediatrics, National Taiwan University Hospital, Taipei, ROC



The most common immunodeficiency in DiGeorge sequence patients is defects in T-cell production due to insufficient thymic tissue. However, because T-lymphocytes are important in regulating antibody responses, DiGeorge sequence is no longer regarded as a pure deficiency of cellular immunity but also a form of variable-combined immunodeficiency. Here we presented a 4-month-old male infant with characteristic facial dysmorphism, thymus dysplasia, tetralogy of Fallot, and documented deletion of chromosome 22q11.2 who had decrease B-lymphocyte numbers and hypogammaglobulinemia. The mitogen responses of T-lymphocytes function were normal with adequate number of CD4+ lymphocytes. This case report highlights the importance of evaluating not only the cellular but also the humoral immune function in patients with DiGeorge sequence.



J Microbiol Immunol Infect 2002;35:187-190.