PiA - Primary Immunodeficiency Association - Common Variable Immunodeficiency CVID, Hypogammaglobulinaemia, Agammaglobulinaemia, Severe Combined Immunodeficiency SCID and X-linked SCID, Neutropenia, Hereditary Angioedema HAE, X-linked agammaglobulinaemia Brutons Disease XLA, Wiskott-Aldrich Syndrome, IgG sub-classes, IgA deficiency, Hyper IgM, Selective IgA deficiency, Selective IgG sub-class deficiences, X-linked Lymphoproliferative Syndrome Duncans Syndrome, C1 esterase inhibitor deficiency, Hyper IgE Syn
Common Variable Immunodeficiency CVID, Hypogammaglobulinaemia, Agammaglobulinaemia, Severe Combined Immunodeficiency SCID and X-linked SCID, Neutropenia, Hereditary Angioedema HAE, X-linked agammaglobulinaemia Brutons Disease XLA, Wiskott-Aldrich Syndrome, IgG sub-classes, IgA deficiency, Hyper IgM, Selective IgA deficiency, Selective IgG sub-class deficiences, X-linked Lymphoproliferative Syndrome Duncans Syndrome, C1 esterase inhibitor deficiency, Hyper IgE Syndrome Jobs Syndrome
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SCID, Severe Combined Immunodeficiency, is a primary immune deficiency. The defining characteristic is usually a severe defect in both the T- & B-lymphocyte systems. This usually results in the onset of one or more serious infections within the first few months of life. These infections are usually serious, and may even be life threatening, they
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