
The primary immunodeficiency disorders reflect abnormalities in the development and maturation of cells of the immune system. These defects result in an increased susceptibility to infection; recurrent pyogenic infections occur with defects of humoral immunity, and opportunistic infections with defects of cell-mediated immunity. These two broad categories of illness correspond roughly to defects in the two principal types of immunocompetent cells, B lymphocytes and T lymphocytes. Defective development of B cells results in abnormalities in humoral immunity, whereas defects in the development of T cells cause problems with cellular immunity. When pathogens are taken up by macrophages or dendritic cells, . . .
Male, X Chromosome, Genetic Linkage, Histocompatibility Antigens Class II, Immunologic Deficiency Syndromes, Wiskott-Aldrich Syndrome, Common Variable Immunodeficiency, Immunoglobulin M, Agammaglobulinemia, Hypergammaglobulinemia, Humans, Female, Severe Combined Immunodeficiency
Male, X Chromosome, Genetic Linkage, Histocompatibility Antigens Class II, Immunologic Deficiency Syndromes, Wiskott-Aldrich Syndrome, Common Variable Immunodeficiency, Immunoglobulin M, Agammaglobulinemia, Hypergammaglobulinemia, Humans, Female, Severe Combined Immunodeficiency
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