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  2. Category:Deaths from sickle-cell disease - Wikipedia

    en.wikipedia.org/wiki/Category:Deaths_from...

    Category:Deaths from sickle-cell disease. Category. : Deaths from sickle-cell disease. This is a non-diffusing subcategory of Category:People with sickle-cell disease. It includes People with sickle-cell disease that can also be found in the parent category, or in diffusing subcategories of the parent.

  3. Splenic sequestration crisis - Wikipedia

    en.wikipedia.org/wiki/Splenic_sequestration_crisis

    Splenic sequestration crisis. Splenic sequestration crisis is a life-threatening illness common in pediatric patients with homozygous sickle cell disease and beta thalassemia. Up to 30% of these children may develop splenic sequestration crisis with a mortality rate of up to 15%. This crisis occurs when splenic vaso-occlusion causes a large ...

  4. Sickle-cell anemia - Wikipedia

    en.wikipedia.org/?title=Sickle-cell_anemia&...

    Language links are at the top of the page. Search. Search

  5. Crizanlizumab - Wikipedia

    en.wikipedia.org/wiki/Crizanlizumab

    Molar mass. 146 232.04 g·mol −1. Crizanlizumab, sold under the brand name Adakveo among others, is a monoclonal antibody medication that binds to P-selectin. [3] It is a medication used to reduce the frequency of vaso-occlusive crisis in people aged 16 years and older who have sickle cell anemia. [3] [4] [6] It is given by injection into a vein.

  6. Point mutation - Wikipedia

    en.wikipedia.org/wiki/Point_mutation

    A single point mutation in this polypeptide chain, which is 147 amino acids long, results in the disease known as Sickle Cell Anemia. Sickle-cell anemia is an autosomal recessive disorder that affects 1 in 500 African Americans, and is one of the most common blood disorders in the United States.

  7. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    Dup - Duplication of a gene or genes. C – Whole chromosome extra, missing, or both (see chromosome abnormality) T – Trinucleotide repeat disorders: gene is extended in length. A cherry red spot, which can be a feature of several storage disorders, including Tay–Sachs disease. Disorder. Chromosome. Mutation.

  8. Vaso-occlusive crisis - Wikipedia

    en.wikipedia.org/wiki/Vaso-occlusive_crisis

    A vaso-occlusive crisis is a common painful complication of sickle cell anemia in adolescents and adults. It is a form of sickle cell crisis. Sickle cell anemia – most common in those of African, Hispanic, and Mediterranean origin – leads to sickle cell crisis when the circulation of blood vessels is obstructed by sickled red blood cells, causing ischemic injuries. The most common ...

  9. James B. Herrick - Wikipedia

    en.wikipedia.org/wiki/James_B._Herrick

    James B. Herrick. James Bryan Herrick (11 August 1861 in Oak Park, Illinois – 7 March 1954 in Chicago, Illinois) was an American physician and professor of medicine who practiced and taught in Chicago. He is credited with the description of sickle-cell disease and was one of the first physicians to describe the symptoms of myocardial infarction .