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  2. IgG4-related disease - Wikipedia

    en.wikipedia.org/wiki/IgG4-related_disease

    Laboratory levels of IgG4 greater than 135 mg/dL Moreover, diagnosis is made due to the presence of painless swellings or mass lesions, or due to complications of masses, e.g. jaundice due to involvement of the pancreas, biliary tree or liver. Symptoms are commonly attributed to other conditions and other diagnoses may have been made years ...

  3. Hypergammaglobulinemia - Wikipedia

    en.wikipedia.org/wiki/Hypergammaglobulinemia

    Hypergammaglobulinemia is a condition that is characterized by the increased levels of a certain immunoglobulin in the blood serum. [1] The name of the disorder refers to an excess of proteins after serum protein electrophoresis (found in the gammaglobulin region). [citation needed]

  4. Immunoglobulin G - Wikipedia

    en.wikipedia.org/wiki/Immunoglobulin_G

    The measurement of immunoglobulin G can be a diagnostic tool for certain conditions, such as autoimmune hepatitis, if indicated by certain symptoms. [18] Clinically, measured IgG antibody levels are generally considered to be indicative of an individual's immune status to particular pathogens.

  5. Autoimmune pancreatitis - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_pancreatitis

    Relatively mild symptoms, such as minimal weight loss or nausea. Increased serum levels of gamma globulins, immunoglobulin G (IgG) or IgG4. The presence of serum autoantibodies such as anti-nuclear antibody (ANA), anti- lactoferrin antibody, anti- carbonic anhydrase II antibody, and rheumatoid factor (RF).

  6. Neuromyelitis optica spectrum disorder - Wikipedia

    en.wikipedia.org/wiki/Neuromyelitis_optica...

    NMOSD brain lesions, as seen under a microscope, show IgG, Immunoglobulin M (IgM), inflammatory cells, and complement deposits around blood vessels. [1] AQP4-IgG is a member of the IgG1 immunoglobulin family, which is an activator of the complement system, which seems to play an integral part in the autoimmune response. [1]

  7. 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.

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    mail.aol.com

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  9. Coombs test - Wikipedia

    en.wikipedia.org/wiki/Coombs_test

    Methyldopa (IgG mediated type II hypersensitivity) Penicillin (high dose) Quinidine (IgM mediated activation of classical complement pathway and Membrane attack complex, MAC) (A memory device to remember that the DAT tests the RBCs and is used to test infants for haemolytic disease of the newborn is: Rh Disease; R = RBCs, D = DAT.)