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  2. Sickle cell disease - Wikipedia

    en.wikipedia.org/wiki/Sickle_cell_disease

    Sickle cell disease (SCD), also simply called sickle cell, is a group of hemoglobin-related blood disorders typically inherited. [2] The most common type is known as sickle cell anemia. [2] It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. [2] This leads to a rigid, sickle -like shape under ...

  3. The Sickle Cell Society - Wikipedia

    en.wikipedia.org/wiki/The_Sickle_Cell_Society

    The Sickle Cell Society , established as a registered charity in 1979, was founded by a group of people with sickle cell disease, their parents and their physicians, aims to improve understanding and management of the condition.

  4. Elizabeth Anionwu - Wikipedia

    en.wikipedia.org/wiki/Elizabeth_Anionwu

    Website. www.elizabethanionwu.co.uk. Dame Elizabeth Nneka Anionwu OM DBE FRCN (born Elizabeth Mary Furlong; 2 July 1947) is a British nurse, health care administrator, lecturer, and Emeritus Professor of Nursing at the University of West London. In 1979, Anionwu became the United Kingdom's first sickle-cell and thalassemia nurse specialist ...

  5. First gene-editing therapy may cure blood disorder - AOL

    www.aol.com/first-gene-editing-therapy-may...

    The treatment for beta thalassaemia is to be offered on the NHS and uses Nobel Prize ... same therapy can be used on the NHS for another genetic disease affecting haemoglobin - sickle cell anaemia

  6. Hemoglobin C - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_C

    Hemoglobin C (abbreviated as HbC) is an abnormal hemoglobin in which glutamic acid residue at the 6th position of the β-globin chain is replaced with a lysine residue due to a point mutation in the HBB gene. [1] People with one copy of the gene for hemoglobin C do not experience symptoms, but can pass the abnormal gene on to their children.

  7. Sickle cell trait - Wikipedia

    en.wikipedia.org/wiki/Sickle_cell_trait

    Hematology. Sickle cell trait describes a condition in which a person has one abnormal allele of the hemoglobin beta gene (is heterozygous), but does not display the severe symptoms of sickle cell disease that occur in a person who has two copies of that allele (is homozygous). Those who are heterozygous for the sickle cell allele produce both ...

  8. Acute chest syndrome - Wikipedia

    en.wikipedia.org/wiki/Acute_chest_syndrome

    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. [1]

  9. Autoimmune hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Autoimmune_hemolytic_anemia

    Autoimmune hemolytic anemia (AIHA) is an autoimmune disorder which occurs when antibodies directed against the person's own red blood cells (RBCs) cause them to burst (lyse), leading to an insufficient number of oxygen-carrying red blood cells in circulation (anemia). The lifetime of the RBCs is reduced from the normal 100–120 days to just a ...

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