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History of Sickle Cell Anemia

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Medical and Surgical Complications of Sickle Cell Anemia
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Abstract

Sickle cell anemia is an inherited disease that existed in Africa for at least 5000 years but there have been no records of its existence till it was discovered in 1904.

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Further Readings

  • Heeney MM, Ware RE. Hydroxyurea for children with sickle cell disease. Pediatr Clin North Am. 2008;55(2):483–501.

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  • Herrick JB. Peculiar elongated and sickle shaped red blood corpuscles in a case of severe anemia. Arch Intern Med. 1910;6:517.

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  • Ingram VM. Gene mutations in human haemoglobins: the chemical difference between normal and sickle cell haemoglobin. Nature. 1957;180:326.

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  • Pauling L, Itano H, Singer SJ, Wells IC. Sickle cell anemia: a molecular disease. Science. 1949;110:543.

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  • Strouse JJ, Lanzkron S, Beach MC, et al. Hydroxyurea for sickle cell disease: a systematic review for efficacy and toxicity in children. Pediatrics. 2008;122(6):1332–42.

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  • Vichinsky EP, Haberkern CM, Neumayr L, et al. A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease. The preoperative transfusion in sickle cell disease study group. N Engl J Med. 1995;333(4):206–13.

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  • Walters MC, Patience M, Leisenring W, et al. Bone marrow transplantation for sickle cell disease. N Engl J Med. 1996;335(6):369–76.

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  • Yawn BP, Buchanan GR, Afenyi-Annan AN, Ballas SK, Hassell KL, James AH, et al. Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members. JAMA. 2014;312(10):1033–48.

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Al-Salem, A. (2016). History of Sickle Cell Anemia. In: Medical and Surgical Complications of Sickle Cell Anemia. Springer, Cham. https://doi.org/10.1007/978-3-319-24762-5_1

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  • DOI: https://doi.org/10.1007/978-3-319-24762-5_1

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-24760-1

  • Online ISBN: 978-3-319-24762-5

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