Sickle Cell Anemia Research Papers

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Sickle Cell Anemia is where the red blood cells become sickle shaped when they are usually supposed to be a round donut shape. The donut shape moves easily through the blood carrying oxygen, where the sickle shape has trouble moving through the blood and can cause problems and pain in the blood vessels. Sickle Cell Anemia is an inherited disease. Each person receives 2 copies of the sickle gene,one from each parent, and this causes abnormal hemoglobin found in sickle cell. Hemoglobin is a protein inside red blood cells which carry oxygen all over the body an gives the blood its red color. When people have sickle cell anemia the abnormal hemoglobin sticks together when it give oxygen to the tissue. People who only inherit one sickle cell gene from there parents will not have sickle anemia, but they will carry the sickle cell trait. When people carry the sickle cell trait they have no symptoms, but like people with sickle cell anemia they can pass this trait on to…show more content…
Anemia is a blood condition where you have a low red blood cell count. Symptoms of Anemia are shortness of breathe, Fatigue, pail skin and nail beds, and also jaundice. The pain is called Sickle Cell Crises. Sickle Cell Crises is where the sickle red blood cells become “C” shaped and get stuck to other “C” shaped cell and cause a block in the blood flow in the capillaries to limbs and organs. The Sickle Cell Crises can cause acute or chronic pain. Acute is more common and can be be very mils or very severe. It lasts anywhere from a few hours to a few days. Chronic pain however last from a few weeks to a few months. Chronic pain is very draining and can limit many activities. Almost every patient with Sickle cell has a painful crises. Some patients have them once a year where others have them 15 or more times a year. The most common places these crises occur are in the bones, abdomen, lungs, and joints blocking blood flow and organ

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