Sickle Cell Anemia, Human Variation And Race
1910 marks the period that sickle-cell anemia was linked to race. In Chicago Dr. James Herrick detailed a “new disorder” that he located in a black patient from the Caribbean who was ill with lesions and fatigue. Dr. Herrick described the illness as “anemia with peculiar and elongated red blood cells”(Tapper, 1). By the 1920s laboratory medicine grew and several other physicians named these elongated red blood cells “sickle-cell.” Sickle-cell disease includes numerous conditions resulting from inheriting the HbS either homozygously or as a compound heterozygote with other abnormal hemoglobin genes (McElroy, 23). During the foundational period for research, physicians who concentrated their work in sickling, “sickle cell trait, a genetic mutation, and sickle cell anemia, the disease that affects persons who inherit the mutated gene from both parents” (Tapper, 1) emphasized racial markers. The fact that the vast majority of people in the United States with sickling are of African descent helps to fuel the inaccurate idea that it is a black phenomenon.Sickling researchers introduce history and geography to explain the disease as “black related.” The most prevalent space for sickling, early observers repo
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Dr Herrick, West Africa, Individuals SS, HbS HbC, America Caribbean, West African, People SS, People HbS, Nigeria Ghana, HbS Malaria, sickle cell, hbs gene, west africa, sickle-cell disease, african origin, cell trait, west african, sickle cell trait, inherited hbs, northern europe, hbs hbc, west african origin, sickle cell gene, inherited hbs gene, europe north america,
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Approximate Word count = 1830
Approximate Pages = 7 (250 words per page double spaced)
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