Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, India

Hum Genet. 1988 Oct;80(2):157-60. doi: 10.1007/BF00702860.

Abstract

We describe here the screening of a small group of apparently healthy individuals belonging to the tribal communities of Koya Dora and Konda Reddi. A remarkably high incidence of deletion and nondeletion alpha + thalassemia mutants has been found with allele frequencies and distributions characteristic to each tribe. We have confirmed the strict relationship between Hb S levels and the number of alpha globin genes in double heterozygotes for the S gene and alpha thalassemia. In this population sample we did not find either heterozygous carriers of alpha 0 thalassemia (deletion of both alpha genes in "cis") or individuals showing hemolytic anemia due to inactivation of three alpha-globin genes (Hb H disease). Selection by malaria is most probably responsible for the prevalence of the various alpha + thalassemia haplotypes among the two tribal populations of Andhra Pradesh.

MeSH terms

  • Ethnicity
  • Globins / genetics*
  • Haplotypes
  • Hemoglobin, Sickle / genetics
  • Heterozygote
  • Humans
  • India
  • Restriction Mapping
  • Sickle Cell Trait / epidemiology
  • Sickle Cell Trait / genetics
  • Thalassemia / epidemiology
  • Thalassemia / genetics*

Substances

  • Hemoglobin, Sickle
  • Globins