27+ Can You Develop Sickle Cell Anemia Later In Life US
27+ Can You Develop Sickle Cell Anemia Later In Life US. This inherited and sometimes serious condition is a hemolytic anemia. Sickle cell anemia is a condition where you do not have enough healthy red blood cells to provide adequate oxygen in your body.
The sickle hemoglobin (hbs) gene is inherited in people of african descent and to a lesser extent in people from the middle east, the mediterranean area, and the aboriginal tribes in india.
Sickle cell anemia is the most severe type of sickle cell disease. Sickle cell disease is not contagious, so you can't catch it from someone else or pass it to another. Infarctions in the spleen, kidneys, bone, cns, and other organs are common and cause progressive loss of organ function and acute and chronic pain in affected parts of the body. The sickle hemoglobin (hbs) gene is inherited in people of african descent and to a lesser extent in people from the middle east, the mediterranean area, and the aboriginal tribes in india.
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