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Indian J Pediatr ; 1997 Mar-Apr; 64(2): 215-9
Article in English | IMSEAR | ID: sea-84300

ABSTRACT

Serum IgG, IgM, IgA, IgG subclasses (IgG1, G2, G3, G4), isohemagglutinins and complement-3 concentrations were measured in 23 beta-thalassemic patients suffering from recurrent infections. No significant abnormalities were found in these humoral immunity investigations, both in splenectomized and non-splenectomized patients. On the other hand, iron overload or repeated blood transfusions were not found to down-regulate the humoral immune system of thalassemic patients.


Subject(s)
Adolescent , Child , Child, Preschool , Complement C3/metabolism , Female , Hemagglutinins/blood , Humans , Immune Tolerance/immunology , Immunoglobulin G/blood , Immunoglobulins/blood , Male , Splenectomy , beta-Thalassemia/diagnosis
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