View Sickle Cell Anemia Answer Key Images. Sickle cell anemia, or sickle cell disease (scd), is a genetic disease of the red blood cells (rbcs). Sickle cell anaemia can damage the spleen, a key organ involved in fighting infection.
B cystic fibrosis C sickle cell anemia D marasmus Answer C ... from www.coursehero.com A chronic hereditary blood disease sickle cell specialized forms as collagen for supportive tissue, hemoglobin for transport, antibodies for immune defense, and enzymes for metabolism protein the fluid that circulates in the principal vascular. These sickle shaped cells get stuck together easily, and block off small blood vessels. Scd can result in significant skeletal muscle remodeling and reduced muscle functional capacities derebail vk, nachman ph, key ns, ansede h, falk rj, kshirsagar av.
It is genetic and tends to show up in the pediatric population.
Sickle cell haemoglobin (hbs) results from an autosomal recessively inherited mutation in which the 17th nucleotide of the beta globin gene is changed. In sickle cell disease, the hemoglobin is abnormal, causing the red blood cells to be rigid and shaped like a c or sickle, the shape from which the disease takes its name. Signs and symptoms of sickle cell anemia usually appear around 5 months of age. When blood can't get to where it should, it can lead to pain and organ people with sickle cell anemia may have jaundice (skin and whites of the eyes look yellow).
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