which there is lower than normal number of red blood cells or hemoglobin within a person‚ consequently decreasing the amount of oxygen being carried to the rest of the body. Causes of such a condition are usually insufficient amounts of iron‚ blood loss‚ lack of red blood cell production‚ or high rates of red blood cell destruction. (MNT‚ http://www.medicalnewstoday.com/articles/158800.php) One form of this condition is the disease Sickle Cell Anemia‚ an inherited blood disorder that affects hemoglobin
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SICKLE CELL ANEMIA Tina Thompson‚ Ashley Scott‚ Araceli Galindo‚ Roshanda Dixon‚ Kristen Wyatt‚ Kimberly Dennis What is Sickle Cell Anemia? Sickle cell anemia is a severe hemolytic anemia resulting in a sickle shaped hemoglobin molecule. It is an inherited disorder with some having sickle cell trait and some having sickle cell disease. The sickle hemoglobin gene is known as the HbS gene. It is found predominantly in people of African descent and occasionally in those of Mediterranean descent
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Sickle cell anemia (SCA) is a genetic disorder that is hereditary. It affects the blood‚ and is caused when the hemoglobin in blood cells are deprived in oxygen from the proteins. These cause normal round blood cells‚ to have are rigid sickle shape. People affected by SCA have a higher risk of death‚ stroke‚ severe attacks‚ and severe rushes of pain. James Herrick discovered an anemia‚ and found bizarre sickle-shaped cells in 1910. A treatment for the disease was discovered in the 1920s by E. Vernon
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Sickle cell anemia is a blood disorder that affects the 11th chromosome which is a hemoglobin gene. Hemoglobin is a protein located in red blood cells (RBCs) that carries oxygen through the body. This disorder is inherited from two parents with abnormal genes that are heterozygous (Rr). This means that both parents who have the trait may pass on the disorder to their offspring. The phenotype makeup is recessive. Those who inherit a normal copy of the chromosome 11 and a mutated chromosome will carry
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families with a history of the autosomal recessive disease Sickle cell anaemia should have all embryos screened with Pre-Implantation Genetic Diagnosis technology (PGD). If tested positive‚ treatment should be made compulsory for the child at a young age and will be treated with stem cell gene therapy. This disease has no personal relevance to me‚ however‚ there is currently 90K people suffering from Sickle cell anaemia in the United States. Sickle cell anaemia is relevant to society because it greatly
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how having sickle cell anemia can make a person more resistant to contracting malaria If it had not been for Anthony Allison‚ the world as we know it today would drastically change. Like the video stated‚ many people with the sickle cell anemia would meet “death before adulthood”. Areas with high frequencies of anopheles mosquito and sickle cell anemia would correlate but nobody would understand why. I admire Allison for not only having the burning inquiry to determine why the sickle cell anemia character
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red blood cells‚ parasites can infect cells carrying defective hemoglobin which may result in death. Allele frequency changes over time depending on the pressures or circumstances facing a particular population. African populations are especially impacted by both malaria and sickle cell anemia. Depending on the impacted population‚ allele frequency often shifts and well suited organisms are likely to survive and allele frequencies can increase. When a population is effected by disease or other
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What is it? Sickle cell anemia is a type of blood disorder that can be inherited from parents. This is when red blood cells that are meant to carry oxygen around the body become deformed. Normal red blood cells are round and disc shaped‚ however‚ when they become sickle red blood cells‚ the deform and change shape into a crescent-like shape or sickle shape. The sickle cells have a shorter life-span than a healthy red blood cell and are not replaced as quickly as normal; this leads to a shortage
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Concept Map: Sickle Cell Disease October 8‚ 2010 Duke University School of Nursing Introduction My client‚ known as 20SE03‚ is a four year old preschooler that lives in a two-parent household along with his younger one year old sister. His family has recently moved to North Carolina where he was recently presented with new onset of seizures and status post cerebral vascular accident (CVA). He has a history of sickle cell disease‚ ulcerative colitis‚ acute chest syndrome‚ and asthma
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SICKLE CELL ANAEMIA Sickle cell anemia is an inherited condition. People with sickle cell anemia inherit two copies of the sickle cell gene‚ one from each parent. The sickle cell gene makes abnormal hemoglobin called Hemoglobin-S. The sickle cell gene is a trait due to a change in ONE nucleotide in the DNA sequence that leads to a change in ONE amino acid that changes how the hemoglobin protein folds. This change in the structure of the hemoglobin protein leads to a change in the shape of
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