Sickle Cell Anemia Case Study - UK Essays.
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Unless we can cure malaria, which based off of my current knowledge, is still a long ways off, then we really shouldn't trying to eradicate the sickle cell trait from the gene pool. In summary, while CRISPR does have the capacity to cure sickle cell anemia, at the present, it is not advisable and simply put, impossible.
The most common type is known as sickle cell anaemia (SCA). It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. This leads to a rigid, sickle -like shape under certain circumstances. Problems in sickle cell disease typically begin around 5 to 6 months of age.
Sickle cell anemia must be better understood in order to accomplish the desired objectives and to recognize the importance of the disease and its limiting factors in addressing patient outcomes. The challenging nature of the disease impacts the health of its patients and requires further evaluation of its pathophysiology and other factors in order to treat the disease with the current.
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Sickle-Cell Anemia Uploaded by FirePits on Oct 20, 2001. Sickle-Cell Anemia is an inherited blood disorder that affects millions of people around the world. It is particularly common among people whose ancestors come from sub-Sahara Africa and Spanish speaking regions. Approximately 2 million Americans carry the sickle cell trait.
Sickle cell anemia is a hereditary disorder that affects countries that were previously affected by malaria - mostly the African Americans and Hispanic Americans (Newland, 2013). The people suffering from this disorder have in the past had barriers to access vital health information and care since it was not covered by the affordable act.