Genetics- Word Count: 214 Sickle cell disease is a genetic blood disorder that plagues millions of people all over the world‚ the highest concentration is found among people of Sub-Saharan African descent. Sickle cell disease is caused by a mutation in the HBB gene located on chromosome 11. Hemoglobin in red blood cells is how oxygen is delivered to cells throughout the body and is composed of four subunits‚ two subunits of alpha- globin and two of beta- globin. The HBB gene provides the instructions
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Sickle cell disease and the hope of stem cell therapies; ethics in the treatment sickle cell. The past half century has been an era of rapid discoveries: from the humble beginnings of molecular biology‚ discovery of the structure of DNA‚ research on recombinant DNA‚ the discovery of the human embryonic stem cell (ESC)‚ the completion of the Human Genome Projects‚ mammalian cloning and the discovery of ntESCs (nuclear transfer ESCs) by somatic cell nuclear transfer and the ethical sigh of relief
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Sickle Cell is an inherited blood disorder that affects approximately 100‚000 people in the United States. Red blood cells contain hemoglobin which is a protein that carries oxygen through the blood. Normal red blood cells are flexible and round. This allows them to travel through the small blood vessels and deliver oxygen to all of the body. Sickle cell disease(SCD) causes these red blood cells to form into a crescent shape‚ like a sickle. The sickle-shaped red blood cells easily break apart‚ causing
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Sickle Cell Plan of Care Read the situation provided. Then‚ provide a brief description of the pathophysiology of sickle cell anemia and complete the nursing care plan by filling in the goals‚ outcomes‚ and nursing orders for the diagnoses provided in the table. SITUATION: Lavon is a 30 year old‚ single African American who was diagnosed with sickle cell anemia when he was 4 years old. He works for a computer company and has been working 12 hour days to meet the deadline for a special project
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General Biology 1 Sickle cell anemia is an inherited disease in which there aren’t enough healthy red blood cells to carry oxygen throughout the body . Where the cell is deformed is in the bone marrow ‚a gene in the bone marrow causes the blood cell to come out in a sickle cell shape because the hemoglobin in the defected body is abnormal‚ after it gives up the oxygen‚ bet together causeing the red blood cells to become to a sickle like shape.People with Sickle cell anemia have abnormal hemoglobin
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Abstract Transitional age youth between the ages of 15-18 who are battling chronic illnesses such as Sickle Cell Disease (SCD) traditionally have a hard time coping to their life style. This causes some to fall into depression and the outlook of the quality of life is decreased also. The eight week study will include six African- American boys and girls from an outpatient clinic that specializes in the medical care of persons with SCD. Participants will meet twice a week for an hour. The Children’s
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Sickle-Cell Disease Greatly affecting the body’s oxygen levels due to mutated red blood cells‚ sickle-cell disease‚ influences an individual’s childhood in multiple ways: cognitive‚ social‚ emotional‚ and physical development. Sickle-cell disease (SCD) refers to an inherited disorder where abnormal hemoglobin is present in one’s red blood cells. Hemoglobin is the protein in red blood cells responsible for carrying oxygen throughout the body. The deformed sickle hemoglobin in people with SCD can form
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Sickle-cell disease‚ also known as sickle-cell anaemia‚ is a hereditary blood disorder‚ caused by an abnormality in the oxygen-carrying protein hemoglobin found in red blood cells. This leads to a propensity for the cells to assume an abnormal‚ rigid‚ sickle-like shape under certain circumstances. Sickle-cell disease is associated with a number of acute and chronic health problems‚ such as severe infections‚ attacks of severe pain‚ stroke‚ and an increased risk of death. Sickle-cell disease occurs
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CELL ULTRASTRUCTURE CELL ULTRASTRUCTURE Cells are the smallest functional units of the body‚ (Waugh‚ A. and Grant‚ A.2010). Most cells are microscopic. The largest cell in the body is the female ovum. The erythrocyte is the smallest cell. The longest cell is the neuron. Cells group together to form tissues‚ each of which has specialised function. Different tissues group together to form organs. Organs are group together to form organ systems‚ each of which performs a particular function that
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Conclusion 1 Based on what you know about blood‚ why would having a sickle cell anemia crisis result in a reduced red blood cell count‚ an elevated white blood cell count‚ and a reduced hematocrit? There’s a reduced RBC count‚ elevated WBC count‚ and a reduced hematocrit because of the shape of the RBC. The sickle cell anemia causes the RBC to have a different shape; a crescent and rigid shape and there are not a lot of them. So because of that‚ there’s more WBC and a reduced hematocrit. Also‚ the
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