beta(S)-Globin gene cluster haplotypes in the West Bank of Palestine

Hemoglobin. 2009;33(2):143-9. doi: 10.1080/03630260902861873.

Abstract

Sickle cell disease is an inherited autosomal recessive disorder of the beta-globin chain. In Palestine it is accompanied by a low level of Hb F (mean 5.14%) and a severe clinical presentation. In this study, 59 Palestinian patients, homozygotes for Hb S were studied for their haplotype background. Eight polymorphic sites in the beta-globin gene cluster were examined. The Benin haplotype was predominant with a frequency of 88.1%, followed by a frequency of 5.1% for the Bantu haplotype. One chromosome was found to carry the Cameroon haplotype (0.85%). Three atypical haplotypes were also found (5.95%). Heterogeneity was observed in Hb F production, ranging between 1.5 and 17.0%, whereas the (G)gamma ratio was homogeneous among all haplotypes with a normal amount of about 41%. Our results are in agreement with previous reports of the Benin haplotype origin in the Mediterranean.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anemia, Sickle Cell / epidemiology*
  • Anemia, Sickle Cell / genetics*
  • Arabs / genetics
  • Female
  • Haplotypes*
  • Hemoglobin, Sickle / genetics*
  • Homozygote
  • Humans
  • Male
  • Middle East / epidemiology
  • Multigene Family
  • Mutation
  • Polymorphism, Genetic
  • beta-Globins / genetics*

Substances

  • Hemoglobin, Sickle
  • beta-Globins