Sickle Cell Anemia: A Curse and a Blessing :: Disease Health Sickness Essays Papers

sickle carrel genus anemia A anathemise and a Blessing reaping hook jail cell anemia is a ailment run ag set right present in America, but in first-class honours degree levels comp atomic number 18d to twain(prenominal) areas of the world. The rate for this ailment is around five times greater in certain places in Africa. That is because the potentially fatal disease reap hook cellular ph one and only(a) Anemia so-and-so also work as a word form of vaccination for an separate disease called malaria. First the mechanics of reap hook carrell Anemia impart be discussed, then its possible benefits. Sickle mobile phone Anemia is an contractable stop. One gene for Sickle Cell Anemia must be inherited from each parent in govern to have the disease. A person who receives a gene for Sickle Cell Anemia from one parent and a normal gene from the other has a condition called reap hook cell trait. Sickle cell trait produces no symptoms or problems for most people. Sick le Cell Anemia foundation neither be contracted nor passed on to other person. The severity of sickle cell disease varies greatly. Some people with sickle cell disease lead lives that are nearly normal. otherwises are less fortunate, and rear touch from a transition of conditions. Sickle Cell Anemia is caused by a assortment in the chemical composition of the protein haemoglobin which is responsible for delivering atomic number 8 throughout our bodies. sane hemoglobin is found as a round shape, and is composed of four proteins two alpha chains and two important chains. The change that causes Sickle Cell Anemia occurs when an amino caustic called valine is substituted for glutamic acid in both of the beta chains. This change in the composure of hemoglobin causes the shape to change when under certain conditions. Two of these conditions are low oxygen and dehydration. The hemoglobin of a person with Sickle Cell Anemia then finds drawn-out and curved, hence the na me sickle cell. When this happens many problems can occur, primarily melody clotting which leads to a lack of oxygen in luggage compartment tissues. Other negative affects of Sickle Cell Anemia are a vitiated heart because it is constantly overworked. Also, bone marrow is change and bones become softer than usual. While there is no cure for Sickle Cell Anemia there is treatment. The primary goal is to reduce the frequency of the Sickle Cell Anemia crisis episodes and maintain enough red filiation cells to keep body tissues healthy.Sickle Cell Anemia A Curse and a Blessing Disease Health Sickness Essays PapersSickle Cell Anemia A Curse and a BlessingSickle Cell Anemia is a disease found right here in America, but in low levels compared to some areas of the world. The rate for this disease is around five times greater in certain places in Africa. That is because the potentially fatal disease Sickle Cell Anemia can also work as a sort of vaccination for another disease c alled malaria. First the mechanics of Sickle Cell Anemia will be discussed, then its possible benefits. Sickle Cell Anemia is an inherited condition. One gene for Sickle Cell Anemia must be inherited from each parent in order to have the disease. A person who receives a gene for Sickle Cell Anemia from one parent and a normal gene from the other has a condition called sickle cell trait. Sickle cell trait produces no symptoms or problems for most people. Sickle Cell Anemia can neither be contracted nor passed on to another person. The severity of sickle cell disease varies greatly. Some people with sickle cell disease lead lives that are nearly normal. Others are less fortunate, and can suffer from a variety of conditions. Sickle Cell Anemia is caused by a change in the chemical composition of the protein hemoglobin which is responsible for delivering oxygen throughout our bodies. Normal hemoglobin is found as a round shape, and is composed of four proteins two alpha chains and two beta chains. The change that causes Sickle Cell Anemia occurs when an amino acid called valine is substituted for glutamic acid in both of the beta chains. This change in the composure of hemoglobin causes the shape to change when under certain conditions. Two of these conditions are low oxygen and dehydration. The hemoglobin of a person with Sickle Cell Anemia then becomes elongated and curved, hence the name sickle cell. When this happens many problems can occur, primarily blood clotting which leads to a lack of oxygen in body tissues. Other negative affects of Sickle Cell Anemia are a weakened heart because it is constantly overworked. Also, bone marrow is affected and bones become softer than usual. While there is no cure for Sickle Cell Anemia there is treatment. The primary goal is to reduce the frequency of the Sickle Cell Anemia crisis episodes and maintain enough red blood cells to keep body tissues healthy.