Dysimmune diseases

• T-, B+, NK- SCID
  29 November 2004

  Etiology
  Locus 5p13
  Locus 11q23
  Locus 19p13.1: germline JAK3 mutations

• severe combined immunodeficiency
  29 November 2004

  SCIDs

• innate immunity
  24 November 2004

  innate immune system, innate immune response, innate immune responses

• immunity
  24 November 2004

  Types
  innate immunity
  acquired immunity
  Pathology
  dysimmunity auto-immunity immune deficiencies WKP
  Definition : In biology, immunity is the balanced state of multicellular organisms having adequate biological defenses to fight infection, disease, or other unwanted biological invasion, while having adequate tolerance to avoid allergy, and autoimmune diseases.
  See also : immune system
  Pathology
  immune deficiencies
  dysimmunity / dysimmune diseases autoimunity / autoimmune (...)

• allergic diseases
  24 November 2004

  See also:
  allergy

• familial juvenile systemic granulomatosis
  22 November 2004

  FJSG, arthrocutaneouveal granulomatosis, ACUG, JABS syndrome, Blau syndrome
  Blau syndrome is a monogenic disease resulting from mutations in nucleotide oligomerization domain 2 (NOD2) and is phenotypically characterized by granulomatous polyarthritis and uveitis.
  The phenotype of Blau syndrome has proven to be more complex than initially thought. The granulomatous character of Blau syndrome provides an opportunity to look at possible pathogenic effects of NOD2 ’gain of function’. (...)

• immunodeficiencies
  22 October 2004

  immune deficiency

• phagocytes
  22 October 2004

  Classification
  neutrophilic polymorphonuclear cells
  macrophages (histiocytes)
  Pathology
  phagocyte defects
  See also
  phagocytosis
  phagolysosome

• Antibodies
  20 October 2004

  antibody

• hereditary angioedemas
  16 September 2004

  hereditary angioneurotic edema, C1 esterase inhibitor deficiency, hereditary angioedemas

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