Reflection:
This is not an aspect of the disease I had thought of before; it is important to remember that there are very human bodies that contain these sickle-shaped cells. The fact that this "treatment" focuses on the symptoms of the disease rather than the cause is also indicative of the difficulty in combating the disease. Comfort is really all that's possible.
Beutler, E. (2002). "Sickle cell disease." Encyclopedia of public health, Vol 4. New York: Macmillan, pp. 1099-100. Retrieved via Gale Cengage.
Summary:
This encyclopedia entry gives a detailed overview of the disease -- it's pathology, causation, prevalence, etc. It begins with a definition of how the disease is classified, both through morphological changes to the red blood cells and, in more recent years, genetic identification. A genetic mutation on the beta-globin gene creates a hemoglobin -- which is a type of protein -- that has less solubility than normal hemoglobin, causing it to build up and clump. The sickle cell gene is now found in almost all populations, but is most prevalent and almost...
Implications for ongoing research into genetic therapies and side effects/later developments are discussed at length. Yannaki, E. & Stamatoyannopoulos, G. (2010). Hematopoietic stem cell mobilization strategies for gene therapy of beta thalassemia and sickle cell disease. Annals of the New York Academy of Sciences 1202: 59-63. Though the clinical trial these two researchers are involved in does not yet have results that are ready for publication, the review of the risks
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