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  2. Poikilocytosis - Wikipedia

    en.wikipedia.org/wiki/Poikilocytosis

    Poikilocytes may be oval, teardrop-shaped, sickle-shaped or irregularly contracted. Normal red blood cells are round, flattened disks that are thinner in the middle than at the edges. A poikilocyte is an abnormally-shaped red blood cell. [1]

  3. Anemia - Wikipedia

    en.wikipedia.org/wiki/Anemia

    The types of anemia treated with drugs are iron-deficiency anemia, thalassemia, aplastic anemia, hemolytic anemia, sickle cell anemia, and pernicious anemia, the most important of them being deficiency and sickle cell anemia with together 60% of market share because of highest prevalence as well as higher treatment costs compared with other ...

  4. Acute chest syndrome - Wikipedia

    en.wikipedia.org/wiki/Acute_chest_syndrome

    The acute chest syndrome is a vaso-occlusive crisis of the pulmonary vasculature commonly seen in people with sickle cell anemia. This condition commonly manifests with a new opacification of the lung(s) on a chest x-ray .

  5. Pappenheimer bodies - Wikipedia

    en.wikipedia.org/wiki/Pappenheimer_bodies

    A cell containing Pappenheimer bodies is a siderocyte. Reticulocytes often contain Pappenheimer bodies. They are mostly observed in diseases such as myelodysplastic syndrome (MDS), sideroblastic anemia, hemolytic anemia, lead poisoning and sickle cell disease. They can interfere with platelet counts when the analysis is performed by electro ...

  6. Voxelotor - Wikipedia

    en.wikipedia.org/wiki/Voxelotor

    Voxelotor has been shown to have disease-modifying potential by increasing hemoglobin levels and decreasing hemolysis indicators in sickle cell patients. [8] It initially appeared to have an acceptable safety profile in sickle cell patients and healthy volunteers, without any dose-limiting toxicity noted in clinical trials. [9]

  7. Hemoglobin - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin

    This variant causes a mild chronic hemolytic anemia. Hemoglobin E (α 2 β E 2) – Another variant due to a variation in the β-chain gene. This variant causes a mild chronic hemolytic anemia. Hemoglobin AS – A heterozygous form causing sickle cell trait with one adult gene and one sickle cell disease gene

  8. Autosplenectomy - Wikipedia

    en.wikipedia.org/wiki/Autosplenectomy

    The most frequent cause of autosplenectomy is sickle cell anemia [10] which causes progressive splenic hypofunction over time. Increased deoxygenation causes sickling of red blood cells, which adhere to the spleen wall and splenic macrophages causing ischemia. [2]

  9. Normocytic anemia - Wikipedia

    en.wikipedia.org/wiki/Normocytic_anemia

    Normocytic anemia is a type of anemia and is a common issue that occurs for men and women typically over 85 years old. Its prevalence increases with age, reaching 44 percent in men older than 85 years. [1] The most common type of normocytic anemia is anemia of chronic disease. [1]