Resumo

MARSAN SUAREZ, Vianed et al. Combined primary inmunodeficiency: a case report. Rev Cubana Hematol Inmunol Hemoter [online]. 2001, vol.17, n.1, pp. 55-58. ISSN 1561-2996.

The case of a 6-year-old boy with recurrent respiratory and digestive infections since he was 8 is reported. The immunological study revealed a marked decrease of the lymphocyte activation, reduced levels of subclasses of IgG2, IgG3 and IgG4 and phagocytosis delay. A combined primary immunodeficiency was diagnosed and it was decided to treat the patient with endovenous gamma globulin, transfer factor and immunoferon. An evident clinical improvement was observed

Palavras-chave : IMMUNOLOGIC DEFICIENCY SYNDROMES; IgG DEFICIENCY; PHAGOCYTOSIS.

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