Primary immunodeficiency

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Revision as of 19:03, 29 August 2019 by Aidan (talk | contribs) (Created page with "* '''Humoural''' (65%): B cell defects ** X-linked agammaglobulinemia ** Common variable immune deficiency (CVID) ** Transient hypogammaglobulinemia of infancy ** Hyper-IgM sy...")
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  • Humoural (65%): B cell defects
    • X-linked agammaglobulinemia
    • Common variable immune deficiency (CVID)
    • Transient hypogammaglobulinemia of infancy
    • Hyper-IgM syndrome
    • IgA deficiency
  • Cell-mediated (5%): T-cell deficiencies
    • DiGeorge syndrome
    • Chronic mucocutaneous candidiasis
  • Combined (15%): B- and T-cell deficiencies, often much more severe
    • Severe combined immunodeficiency disease (SCID)
    • Wiskott-Aldrich syndrome
    • Ataxia-telangiectasia
    • X-linked lymphoproliferative disease
  • Phagocytic (10%): neutrophil deficiencies
    • Phagocyte deficiencies
    • Chronic granulomatous disease (CGD)
    • Leukocyte adhesion deficiency
  • Complement (5%)
    • C2 deficiencies