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  2. Pancytopenia - Wikipedia

    en.wikipedia.org/wiki/Pancytopenia

    Pancytopenia is a medical condition in which there is significant reduction in the number of almost all blood cells (red blood cells, white blood cells, platelets, monocytes, lymphocytes, etc.). If only two parameters from the complete blood count are low, the term bicytopenia can be used.

  3. Cytopenia - Wikipedia

    en.wikipedia.org/wiki/Cytopenia

    Pancytopenia – when all three types of blood cells; red blood cells, white blood cells, and platelets, are all deficient. This is a life-threatening disorder that is a characteristic of aplastic anemia .

  4. Hemophagocytic lymphohistiocytosis - Wikipedia

    en.wikipedia.org/wiki/Hemophagocytic_lymphohist...

    This is a rare autosomal recessive disorder characterized by partial albinism, hepatosplenomegaly, pancytopenia, hepatitis, immunologic abnormalities, and lymphohistiocytosis. Most cases have been diagnosed between 4 months and 7 years of age, with a mean age of about 17 months. [citation needed]

  5. Reticulocytopenia - Wikipedia

    en.wikipedia.org/wiki/Reticulocytopenia

    If pancytopenia is present, bone marrow failure [4] must be considered and evaluation for bone marrow failure syndromes or aplastic anemia must be pursued. Treatment is dependent on the etiology and may include replacement of blood products as patients can develop severe anemia.

  6. Gaucher's disease - Wikipedia

    en.wikipedia.org/wiki/Gaucher's_disease

    Hypersplenism and pancytopenia, the rapid and premature destruction of blood cells, leads to anemia, neutropenia, leukopenia, and thrombocytopenia (with an increased risk of infection and bleeding). Cirrhosis of the liver is rare. Severe pain associated with joints and bones occurs, frequently presenting in hips and knees.

  7. Paroxysmal nocturnal hemoglobinuria - Wikipedia

    en.wikipedia.org/wiki/Paroxysmal_nocturnal...

    Danicopan, sold under the brand name Voydeya, is a medication used for the treatment of paroxysmal nocturnal hemoglobinuria. It is a complement inhibitor which reversibly binds to factor D to prevent alternative pathway-mediated hemolysis and deposition of complement C3 proteins on red blood cells. The most common side effects include fever, headache, increased levels of liver enzymes (a sign ...

  8. Felty's syndrome - Wikipedia

    en.wikipedia.org/wiki/Felty's_syndrome

    Felty's syndrome (FS), also called Felty syndrome, [1] is a rare autoimmune disease characterized by the triad of rheumatoid arthritis, enlargement of the spleen and low neutrophil count.

  9. Evans syndrome - Wikipedia

    en.wikipedia.org/wiki/Evans_syndrome

    Evans syndrome is an autoimmune disease in which an individual's immune system attacks their own red blood cells and platelets, the syndrome can include immune neutropenia. [1] [2] These immune cytopenias may occur simultaneously or sequentially.