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Sickle cell Diseases are a group of hereditary blood disorders, which affects hemoglobin a molecule in charge of delivering oxygen through the body. Most of the disease cause by Sickle cell disease are due to a genetic change in hemoglobin. Worldwide proximally one in every 2500,000 babies are born with sickle cell disease. In the USA 20K to 200K are affected with sickle cell disease, the most affected population are Latin American and African Americans.
The sickle cell gene is passed from generation to generation, this means that both the father and the mother must pass on the imperfect form of the gene for a kid to be affected. An ideally working hemoglobin carries oxygen from the lungs to the different tissues throughout the body. Sickle hemoglobin can also carry oxygen. However, once the oxygen is liberated, sickle hemoglobin transform into rigid rods that alter the shape of the red blood cell. Sickle cells have a small life span in comparison to normal red blood cells. Normal red blood cells survive for around 120 days in the bloodstream, sickle cells survive for only 10-12 days. As a result, the bloodstream is very short of red blood cells and hemoglobin, and as the result an affected individual develops Sickle cell anemia.
The sickle cells can create other …show more content…
Treatments are made to help relieve symptoms and treat complications. The goals of treating the diseases are to make the life of the patent better by relieving pain; preventing infections, organ damage, strokes; and control complications (if any). There are a lot of practices that are made to prevent some of the symptoms and complications of sickle cell disease. These involve preventative antibiotics, good hydration, and immunization. Maintaining good health through proper nutrition, avoiding stresses and infection, as well as getting proper rest are also important. If a patient follows this steps they will most likely see improvement on their overall

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