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Distribution of Sickle-cell Hæmoglobin in Saudi Arabia

Abstract

IT is now recognized that the sickle-cell trait, though inherited through a single gene, does not necessarily maintain a constant frequency in a population from, generation to generation, but that its frequency is the result of two opposing processes of natural selection. The gene for sickle-cell hæmoglobin (or hæmoglobin S) tends to be eliminated from the population because of the deaths of homozygotes from sickle-cell anæmia, while, in the presence of endemic falciparum (malignant tertian) malaria, homozygotes for normal adult hæmoglobin (hæmoglobin A) have a higher mortality than heterozygotes with genes for both A and S. The sickle-cell gene is thus maintained from generation to generation from the pool represented by the favoured heterozygotes. So long as malarial incidence remains constant, a state of balanced polymorphism will eventually be reached; but if the former then changes, there will be a gradual shift towards a new balance of genes. There can, therefore, be no doubt that the frequency of the sickle-cell trait in a population is, at least in part, related to the recent malarial history of that population.

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References

  1. Daggy, R. H., Amer. J. Trop. Med., 8, 286 (1960).

    Google Scholar 

  2. Lehmann, H., Eug. Rev., 46, 3 (1954).

    Google Scholar 

  3. Coon, C. S., The Races of Europe, 425 (New York, 1948).

    Google Scholar 

  4. Lehmann, H., Sharih, A., and Robinson, G. L., Man, 61, 108 (1961).

    Article  Google Scholar 

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LEHMANN, H., MARANJIAN, G. & MOURANT, A. Distribution of Sickle-cell Hæmoglobin in Saudi Arabia. Nature 198, 492–493 (1963). https://doi.org/10.1038/198492b0

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