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114 Possible Causes for Hyper IgA

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  • Vasculitis

    . • Immunoglogulin levels (IgG, M, A)- Usually hyper gammaglobulinemia seen- Elevated IgA levelsHenoch Sconlein Purpura• Cryoglobulins- Essential Mixed Cryoglobulinemia•[]

  • Primary Immune Deficiency Disorder

    IgM syndrome IgG subclass deficiency and specific antibody deficiency Omenn syndrome Selective IgA deficiency Severe combined immune deficiency Wiskott-Aldrich syndrome X-linked[] ) agammaglobulinemia Chronic granulomatous disease Hyper-IgE Syndrome (STAT-3 deficiency) DiGeorge Syndrome Periodic fever syndromes / autoinflammatory syndromes[] […] syndrome Hyper-IgM syndrome DiGeorge syndrome IgG subclass deficiency and specific antibody deficiency Ataxia telangiectasia Hyper-IgE syndrome Complement deficiencies Interleukin[]

  • Crohn's Disease

    X-linked hyper-immunoglobulin M (IgM) syndrome is characterized by recurrent infections, low or undetectable levels of IgG and IgA, and normal to increased serum IgM, and[]

  • Growth Hormone Deficiency

    […] serum levels of IgG and IgA and an elevated serum level of IgM).[] We report the case of a patient with a history of recurrent diarrhea and respiratory infections diagnosed with hyper IgM syndrome on the basis of immunological findings (low[]

  • Chronic Glomerulonephritis

    As to the pathogenesis, we found that CB4 provoked exacerbation of renal pathologic findings in hyper IgA mice via endothelial injury, γ-interferon production, and dysfunction[]

  • Lymphadenitis

    G (IgG) and IgA, and normal/increased serum levels of IgM.[] Abstract The hyper-immunoglobulin M (HIGM) syndrome is a heterogeneous group of genetic disorders characterized by recurrent infections, decreased serum levels of immunoglobulin[]

  • Ulcerative Colitis

    FEMS Microbiology Ecology, in press. (32) Hashizume, K., Tsukahara, T., Yamada, K., Koyama, H., and Ushida, K. (2003) Megasphaera elsdenii JCM1772T normalizes hyper-lactate[] Disease 14: 241-246. (31) Inoue, R. and Ushida K.(2003) Development of the intestinal microbiota in rats and its possible interactions with the evolution of the luminal IgA[]

  • Eosinophilic Endomyocardial Disease

    Immune deficiencies, such as hyper-IgE syndrome, hyper-IgM syndrome, and IgA deficiency, can lead to eosinophilia.[]

  • Hereditary Hyperekplexia

    PS275200 Hypotonia, infantile, with psychomotor retardation and characteristic facies PS615419 Hypotrichosis PS605389 Ichthyosis, congenital, autosomal recessive PS242300 IgA[] […] nephropathy PS161950 Immunodeficiency (Select Examples) PS300755 Immunodeficiency with hyper-IgM PS308230 Immunodeficiency, common variable PS607594 Immunodeficiency-centromeric[]

  • Henoch-Schönlein Purpura

    Hyper-reactivity of both B and T cells in response to specific antigenic stimuli in vitro has been reported in patients with IgA nephropathy and HSP ( 8 ).[]

Further symptoms