When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Medical genetics of Jews - Wikipedia

    en.wikipedia.org/wiki/Medical_genetics_of_Jews

    This would be similar to the hemoglobin allele which is responsible for sickle-cell disease, but solely in people with two copies; those with just one copy of the allele have a sickle cell trait and gain partial immunity to malaria as a result. This effect is called heterozygote advantage. [27]

  3. File:Sickle Cell Anemia and its Protection Against Malaria.svg

    en.wikipedia.org/wiki/File:Sickle_Cell_Anemia...

    English: In series A the red blood cell becomes sickled after interaction with the malarial merozoite, which then begins to multiply in the cell (schizont). Due to the heterozygous nature of the cell, and the hemoglobin inside it causing sickling, likely as a result of the lowering of the pH and deoxygenation, the cell can be targeted and eliminated by macrophages before the infection can ...

  4. Elizabeth Anionwu - Wikipedia

    en.wikipedia.org/wiki/Elizabeth_Anionwu

    She travelled to the United States to study counselling for sickle-cell and thalassemia centres as courses were not then available in the UK. In 1979 she worked with Dr Milica Brozovic to create the first UK sickle-cell and thalassemia counselling centre in London Borough of Brent. This was the first of over 30 centres in the UK using the Brent ...

  5. Graham Roger Serjeant - Wikipedia

    en.wikipedia.org/wiki/Graham_Roger_Serjeant

    All 550 cases of sickle-cell disease were identified and along with 250 normal matched controls have now been followed for up to 48 years. Thanks to the advantages of an island and an intelligent cooperative population, virtually all surviving cases of the disease continue to be monitored and the study has told the world much about sickle-cell ...

  6. 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.

  7. 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.

  8. Echinocyte - Wikipedia

    en.wikipedia.org/wiki/Echinocyte

    Scanning electron microscopy (SEM) of echinocytes Echinocyte compared to other forms of poikilocytosis. Echinocyte (from the Greek word echinos, meaning 'hedgehog' or 'sea urchin'), in human biology and medicine, refers to a form of red blood cell that has an abnormal cell membrane characterized by many small, evenly spaced thorny projections.

  9. Renal medullary carcinoma - Wikipedia

    en.wikipedia.org/wiki/Renal_medullary_carcinoma

    Renal medullary carcinoma is a rare type of cancer that affects the kidney.It tends to be aggressive, difficult to treat, and is often metastatic at the time of diagnosis. . Most individuals with this type of cancer have sickle cell trait or rarely sickle cell disease, suggesting that the sickle cell trait may be a risk factor for this type of ca