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  2. Hyper IgM syndrome - Wikipedia

    en.wikipedia.org/wiki/Hyper_IgM_syndrome

    Hyper IgM syndrome is a rare primary immune deficiency disorders characterized by low or absent levels of serum IgG, IgA, IgE and normal or increased levels of serum IgM. [ 8 ] They are resulting from mutations in the pathway from B-cell activation to isotype class switching.

  3. Immunoglobulin M - Wikipedia

    en.wikipedia.org/wiki/Immunoglobulin_M

    Immunoglobulin M (IgM) is the largest of several isotypes of antibodies (also known as immunoglobulin) that are produced by vertebrates. IgM is the first antibody to appear in the response to initial exposure to an antigen ; [ 1 ] [ 2 ] causing it to also be called an acute phase antibody.

  4. Hyper-IgM syndrome type 4 - Wikipedia

    en.wikipedia.org/wiki/Hyper-IgM_syndrome_type_4

    Hyper IgM syndromes is a group of primary immune deficiency disorders characterized by defective CD40 signaling; via B cells affecting class switch recombination (CSR) and somatic hypermutation. Immunoglobulin (Ig) class switch recombination deficiencies are characterized by elevated serum IgM levels and a considerable deficiency in ...

  5. Immunodeficiency with hyperimmunoglobulin M - Wikipedia

    en.wikipedia.org/wiki/Immunodeficiency_with...

    Immunodeficiency with hyperimmunoglobulin M is a rare disorder characterized by recurrent infections, low or absent IgG, IgE, and IgA levels, and normal or elevated levels of IgM and IgD. [ 2 ] : 84

  6. Waldenström macroglobulinemia - Wikipedia

    en.wikipedia.org/wiki/Waldenström_macroglobulinemia

    It is characterized by having high levels of a circulating antibody, immunoglobulin M (IgM), which is made and secreted by the cells involved in the disease. Waldenström macroglobulinemia is an "indolent lymphoma" (i.e., one that tends to grow and spread slowly) and a type of lymphoproliferative disease which shares clinical characteristics ...

  7. Hypergammaglobulinemia - Wikipedia

    en.wikipedia.org/wiki/Hypergammaglobulinemia

    Immunodeficiency with hyper IgM type 2 is caused by a mutation in the Activation-Induced Cytidine Deaminase gene, which is located on the short arm of chromosome 12.. The protein that is encoded by this gene is called Activation-Induced Cytidine Deaminase (AICDA) and functions as a DNA-editing deaminase that induces somatic hypermutation, class switch recombination, and immunoglobulin gene ...

  8. Anti-MAG peripheral neuropathy - Wikipedia

    en.wikipedia.org/wiki/Anti-MAG_peripheral_neuropathy

    Anti-MAG antibodies can be readily detected in a patient's sera using various types of assays, but mainly an ELISA has been shown to be most effective. [1] [8] There are also various biological indicators, such as elevated cerebral spinal fluid proteins and elevated IgM monoclonal levels.

  9. Coombs test - Wikipedia

    en.wikipedia.org/wiki/Coombs_test

    Since these antibodies sometimes destroy red blood cells they can cause anemia; this test can help clarify the condition. The indirect Coombs test detects antibodies that are floating freely in the blood. [1] These antibodies could act against certain red blood cells; the test can be carried out to diagnose reactions to a blood transfusion. [1]