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  2. Hereditary persistence of fetal hemoglobin - Wikipedia

    en.wikipedia.org/wiki/Hereditary_persistence_of...

    In persons with sickle cell disease, high levels of fetal hemoglobin as found in a newborn or as found abnormally in persons with hereditary persistence of fetal hemoglobin, the HbF causes the sickle cell disease to be less severe. In essence the HbF inhibits polymerization of HbS. A similar mechanism occurs with persons who have sickle cell trait.

  3. Microcytic anemia - Wikipedia

    en.wikipedia.org/wiki/Microcytic_anemia

    Microcytic anaemia; Microcytosis is the presence of red cells that are smaller than normal. Normal adult red cell has a diameter of 7.2 µm. Microcytes are common seen in with hypochromia in iron-deficiency anaemia, thalassaemia trait, congenital sideroblastic anaemia and sometimes in anaemia of chronic diseases.

  4. Hemoglobin A2 - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_A2

    Hemoglobin A2 (HbA 2) is a normal variant of hemoglobin A that consists of two alpha and two delta chains (α 2 δ 2) and is found at low levels in normal human blood.Hemoglobin A2 may be increased in beta thalassemia or in people who are heterozygous for the beta thalassemia gene.

  5. Umut A. Gurkan - Wikipedia

    en.wikipedia.org/wiki/Umut_A._Gurkan

    In this role, he focused his research on sickle cell disease and earned numerous grants to fund his studies. In December 2013, his research team received a Doris Duke Foundation award to "discover how to predict when sickle cell disease patients will suffer an acute crisis and monitor the effectiveness of treatments."

  6. Hemoglobin E - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_E

    Compound heterozygotes with sickle-hemoglobin E disease result when the gene of hemoglobin E is inherited from one parent and the gene for hemoglobin S from the other. As the amount of fetal hemoglobin decreases and hemoglobin S increases, a mild hemolytic anemia appears in the early stage of development.

  7. Sickle cell retinopathy - Wikipedia

    en.wikipedia.org/wiki/Sickle_cell_retinopathy

    Proliferative sickle retinopathy is the most severe ocular complication of sickle cell disease. Even though PSCR begins in the first decade of life, the condition remains asymptomatic and unnoticed until visual symptoms occur due to vitreous hemorrhage or retinal detachment.

  8. Hairy cell leukemia - Wikipedia

    en.wikipedia.org/wiki/Hairy_cell_leukemia

    Hairy cell leukemia is an uncommon hematological malignancy characterized by an accumulation of abnormal B lymphocytes. [1] It is usually classified as a subtype of chronic lymphocytic leukemia (CLL). Hairy cell leukemia makes up about 2% of all leukemias, with fewer than 2,000 new cases diagnosed annually in North America and Western Europe ...

  9. Grimace scale - Wikipedia

    en.wikipedia.org/wiki/Grimace_scale

    A drawing by Konrad Lorenz showing facial expressions of a dog. The grimace scale (GS), sometimes called the grimace score, is a method of assessing the occurrence or severity of pain experienced by non-human animals according to objective and blinded scoring of facial expressions, as is done routinely for the measurement of pain in non-verbal humans.