Studyspark Study Document

Sickle Cell Anemia There Are Term Paper

Pages:5 (1736 words)

Sources:5

Subject:Health

Topic:Sickle Cell Anemia

Document Type:Term Paper

Document:#83160177


These crises are a direct result of way in which the deformed red blood cells adhere to both each other and the insides of the blood vessel walls, blocking tissues from receiving oxygen. The disease is prevalent across some parts of Africa, the Middle East and India, which is due to the way in which the heterozygous form of the condition offers carriers a degree of protection against malaria, which is present in these areas. As a result, there is also a significant incidence of the disease in African-Americans, as a direct result of their African heritage, which means that the condition is significantly important for practitioners across the U.S. To understand.

References

Chowning, J.T. (2000) Sickle cell anemia and genetics: Background information. Washington State University Website. Retrieved on June 18, 2007, at http://genetics-education-partnership.mbt.washington.edu/.

Frenette, P.S. And Atweh, G.F. (2007) Sickle cell disease: Old discoveries, new concepts and future promises. Journal of Clinical Investigation, 117, 850-858.

Ingram, V.M. (2004) Sickle-cell anemia hemoglobin: The molecular biology of the first "molecular disease" - the crucial importance of serendipity. Genetics, 167, 1-7.

Nagel, R.L. (2005) Sickle Cell Anaemia. Encyclopedia of Life Sciences, John Wiley and Sons. Retrieved June 18, 2007, from:

Steinberg, M.H. (2005) Sickle cell disease as a multifactorial condition. Encyclopedia of Life Sciences, John Wiley and Sons. Retrieved June 18, 2007, from:

Weatherall, D.J. (1997) ABC of clinical haematology: The…


Sample Source(s) Used

References

Chowning, J.T. (2000) Sickle cell anemia and genetics: Background information. Washington State University Website. Retrieved on June 18, 2007, at http://genetics-education-partnership.mbt.washington.edu/.

Frenette, P.S. And Atweh, G.F. (2007) Sickle cell disease: Old discoveries, new concepts and future promises. Journal of Clinical Investigation, 117, 850-858.

Ingram, V.M. (2004) Sickle-cell anemia hemoglobin: The molecular biology of the first "molecular disease" - the crucial importance of serendipity. Genetics, 167, 1-7.

Nagel, R.L. (2005) Sickle Cell Anaemia. Encyclopedia of Life Sciences, John Wiley and Sons. Retrieved June 18, 2007, from:

Cite this Document

Join thousands of other students and "spark your studies."

Sign Up for FREE
Related Documents

Studyspark Study Document

Sickle Cell Anemia Is an

Pages: 4 (1267 words) Sources: 1+ Subject: Genetics Document: #89643594

For example, in the case of sickle beta thalassemia, the individual has inherited a gene for hemoglobin S. from one parent and a gene for beta-thalassemia from the other. Or, in the instance of SC disease, the individual has inherited a gene for hemoglobin S. from one parent and a gene for hemoglobin C. from the other. The sickle cell trait in heterozygous carriers confers the resistance to malaria phenotype

Studyspark Study Document

Sickle Cell Anemia

Pages: 2 (617 words) Subject: Disease Document: #81837801

Sickle Cell Anemia There are both advantages and disadvantages of having sickle cell anemia. How much benefit a person gets from sickle cell anemia's advantages, however, largely depends on where that person is located and what his or her environment is. The same concept applies to the disadvantages of this condition, although to a lesser extent. The root of the advantages and disadvantages of this disease pertain to its specific form

Studyspark Study Document

Sickle Cell Anemia

Pages: 3 (891 words) Sources: 1+ Subject: Disease Document: #52165544

Sickle Cell (Rough Draft) Sickle cell anemia is a blood disease that causes badly formed red blood cells. The disease is genetec. Mostly people from Africa or other coutries around the Mediterraean Sea get it. In the United States, African-Americans are most likely to have it (Howard, 1995). Red blood cells are the blood cells that carry oxygen throughout the body. When a person has sickle-cell anemia the hemoglobon in the cell

Studyspark Study Document

Sickle Cell Anemia According to the U.S.

Pages: 2 (574 words) Sources: 1 Subject: Disease Document: #55336818

Sickle cell anemia according to the U.S. National Library of Medicine/National Institutes of Health - NLM/NIH (2013), "is a disease in which your body produces abnormally shaped red blood cells." As the NLM/NIH further point out, the cells produced in this case ordinarily have a crescent-like shape. The red blood cells of an individual usually have a disk-like shape. It is this disk like shape that enhances and eases their

Studyspark Study Document

Sickle Cell Anemia As an Inherited Condition,

Pages: 4 (1404 words) Sources: 5 Subject: Disease Document: #25535958

Sickle Cell Anemia As an inherited condition, it is presence of hemoglobin which tends to be abnormal that brings about sickle cell anemia. In basic terms, hemoglobin is a red blood cell protein whose main function is carrying oxygen. It is this hemoglobin abnormality that informs 'sickled' or distorted red blood cells whose survival is compromised as a result of the distortion and fragility. Though the prevalence of the condition largely

Studyspark Study Document

Sickle Cell Anemia Definition and

Pages: 11 (3168 words) Sources: 1+ Subject: Disease Document: #9653958

Another symptom that is often found is a yellowing of skin and eyes; this is a sign of jaundice due to the breakdown of red blood cells. Another sign is that children may show delayed growth and development. (Genetic Disease Profile: Sickle Cell Anemia) One of the aspects that problematizes this disease are the complications that can arise as a result of the lowering of body defenses and the increased

Join thousands of other students and

"spark your studies".