Sickle Cell Anemia Sickle Cell Anemia is a blood disorder that shortens the life span of red blood cells‚ and eventually the organisms they are located in. Sickle Cell Anemia is an inherited blood disorder that changes that structure of red blood cells. In a healthy organism‚ red blood cells are disk shaped and move easily through the blood vessels. In an organism that has sickle cell anemia the red blood cells’ structures are corrupted; instead of the disk-like shape‚ the red blood cells have
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Sickle cell anemia is an inherited blood disorder that cause the abnormal formation of the hemoglobin protein in red blood cells (Nih). Hemoglobin is an essential protein that resides within the red blood cells supplying oxygen to the entire body. Hemoglobin S causes a mutation in shape of hemoglobin protein causing a group of blood disorders including sickle cell anemia and thalassemia. Sickle cell anemia is a result of one abnormal hemoglobin S gene given to a child by each parent‚ children that
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Anemia Iron deficiency anemia is a blood disease where your body does not have sufficient iron to make red blood cells. Red blood cells are important for the body to provide oxygen to your brain and tissues. If the body does not have sufficient iron‚ the blood provided to the brain and tissues cannot be carried efficiently. The human body normally gets iron from the consumption of high iron food‚ and or from old red blood cells. Iron deficiency anemia can occur when the body loses blood cells at
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Adams 1 Dwayne Adams Instructor: Croshaw Medical Terminology 1 18‚ April 2013 Sickle Cell Anemia Sickle-cell Anemia is a genetic blood disorder caused by the presence of an abnormal form of hemoglobin molecules in which the red blood cells loose their disc-shape and become crescent shaped. The shape also known as “hemoglobin S”. unlike normal red cells which are usually smooth and malleable‚ tend to collect after releasing oxygen‚ and cannot squeeze through small blood vessels. The
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Sickle cell anemia is a genetic disease that affects the shape and functionality of red blood cells. It is caused by a mutation in the DNA of the protein‚ hemoglobin‚ specifically in the beta chain. There are 531 base pairs in this DNA strand. Substitution or point mutation occurs‚ causing “GAG” to become “GTG”. This results in valine being created instead of glutamate. The mutation causes the hemoglobin to cling together in low oxygen levels and the red blood cell changes shape‚ preventing it from
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Sickle Cell Anemia first came into the view of the world around 1910 when Dr. James Herrick; a cardiologist‚ had a patient who complained of pain and described symptoms that sounded like anemia. He handed the case down to his assistant who‚ after taking a blood sample‚ discovered that the patient’s blood cells were not shaped like normal blood cells. When the patient’s blood cells were compared to normal blood cells‚ they appeared to be “sickle shaped”. After seeing this for himself Dr. Herrick took
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Thalassemia and what they need in order to survive. After reading this essay you will see how you‚ can help them live. Thalassemia is a genetic blood disease in which the amount of hemoglobin is too low or too high which then leads to microcytic anemia. Hemoglobin is a red protein that transports oxygen in the blood. Each molecule contains iron atom that is bound to a heme group. Scientists have predicted that this disease will be worldwide in the next century but now it’s most common in the Mediterranean
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Congenital Spherocytic Anemia‚ also known as Hereditary Spherocytosis is a rare blood condition I have had since my birth and this is why I wanted to research it. A lot of people have a hard time understanding what this condition is and what effects it has on a person; it requires a lot of in depth information to get a full understanding. Hereditary Spherocytosis is a red blood cell disorder which changes the shape of the cells to be spherical‚ which causes a lot of complications. The Outcome was
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Erythrocyte count = 3.1 x 10/mm RBC smear showed microcytic and hypochromic cells Reticulocyte count = 1.5% Other laboratory values were within normal limits. Question Considering the circumstances and the preliminary workup‚ what type of anemia does Ms. A most likely have? In an essay of 500-750 words‚ explain your answer and include rationale. Case Study #2 Mr. P is a 76-year-old male with cardiomyopathy and congestive heart failure who has been hospitalized frequently to treat CHF
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Critical Care Nursing: Sickle Cell Anemia Critical Care Nursing 10/15/2009 Sickle cell anemia affects millions of people worldwide. Sickle cell anemia is a disease in which your body produces abnormally shaped red blood cells. They don’t last as long as normal‚ round red blood cells‚ which leads to anemia. Sickle cells contain abnormal hemoglobin that causes the cells to have a sickle shape. Sickle-shaped cells don’t move easily through your blood vessels. They’re
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