Gamer.Site Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Cold agglutinin disease - Wikipedia

    en.wikipedia.org/wiki/Cold_agglutinin_disease

    Hematology. Cold agglutinin disease ( CAD) is a rare autoimmune disease characterized by the presence of high concentrations of circulating cold sensitive antibodies, usually IgM and autoantibodies that are also active at temperatures below 30 °C (86 °F), [ 1] directed against red blood cells, causing them to agglutinate and undergo lysis ...

  3. Non-contact thermography - Wikipedia

    en.wikipedia.org/wiki/Non-contact_thermography

    ICD-9. 88.8. MeSH. D013817. [ edit on Wikidata] Non-contact thermography, thermographic imaging, or medical thermology is the field of thermography that uses infrared images of the human skin to assist in the diagnosis and treatment of medical conditions. Medical thermology is sometimes referred to as medical infrared imaging or tele-thermology ...

  4. Warm antibody autoimmune hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Warm_antibody_autoimmune...

    Warm antibody autoimmune hemolytic anemia ( WAIHA) is the most common form of autoimmune haemolytic anemia. [ 1] About half of the cases are of unknown cause, with the other half attributable to a predisposing condition or medications being taken. Contrary to cold autoimmune hemolytic anemia (e.g., cold agglutinin disease and paroxysmal cold ...

  5. Coombs test - Wikipedia

    en.wikipedia.org/wiki/Coombs_test

    The direct Coombs test is used to detect antibodies or complement proteins attached to the surface of red blood cells. To perform the test, a blood sample is taken and the red blood cells are washed (removing the patient's plasma and unbound antibodies from the red blood cells) and then incubated with anti-human globulin ("Coombs reagent").

  6. Hereditary haemochromatosis - Wikipedia

    en.wikipedia.org/wiki/Hereditary_haemochromatosis

    Atransferrinemia. Hereditary haemochromatosis type 1 ( HFE-related haemochromatosis) [ 3] is a genetic disorder characterized by excessive intestinal absorption of dietary iron, resulting in a pathological increase in total body iron stores. [ 4] Humans, like most animals, have no mechanism to regulate excess iron, simply losing a limited ...

  7. Plummer–Vinson syndrome - Wikipedia

    en.wikipedia.org/wiki/Plummer–Vinson_syndrome

    Plummer–Vinson syndrome (also known as Paterson–Kelly syndrome [1] or Paterson–Brown-Kelly syndrome in the UK [2]) is a rare disease characterized by dysphagia (difficulty swallowing), iron-deficiency anemia, glossitis (inflammation of the tongue), cheilosis (cracking at the corners of the mouth), and esophageal webs (thin membranes in the esophagus that can cause obstruction). [1]

  8. Aplastic anemia - Wikipedia

    en.wikipedia.org/wiki/Aplastic_anemia

    In aplastic anemia, the patient has pancytopenia (i.e., also leukopenia and thrombocytopenia) resulting in a decrease of all formed elements. In contrast, pure red cell aplasia is characterized by a reduction in red cells only. The diagnosis can only be confirmed with a bone marrow examination. [citation needed]

  9. Cold autoimmune hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Cold_autoimmune_hemolytic...

    Pathophysiology. Cold agglutinins, or cold autoantibodies, occur naturally in nearly all individuals. These natural cold autoantibodies occur at low titers, less than 1:64 measured at 4 °C, and have no activity at higher temperatures. Pathologic cold agglutinins occur at titers over 1:1000 and react at 28-31 °C and sometimes at 37 °C.