Beta-globin gene cluster haplotypes and alpha-thalassemia in sickle cell disease patients from Trinidad

Autor: Marc Romana, Erskine Smith, Lisiane Kéclard, Altheia Jones-Lecointe, Marie-Georges Gilbert, C. Saint-Martin, Waveney P. Charles
Přispěvatelé: Biologie Intégrée du Globule Rouge (BIGR (UMR_S_1134 / U1134)), Institut National de la Transfusion Sanguine [Paris] (INTS)-Université de La Réunion (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pointe-à-Pitre/Abymes [Guadeloupe] -Université des Antilles (UA)-Université de Paris (UP)
Rok vydání: 2008
Předmět:
Zdroj: American Journal of Human Biology
American Journal of Human Biology, Wiley, 2008, 20 (3), pp.342-344. ⟨10.1002/ajhb.20732⟩
ISSN: 1520-6300
1042-0533
DOI: 10.1002/ajhb.20732⟩
Popis: International audience; In this study, we have determined the frequency of beta(S) haplotypes in 163 sickle cell disease patients from Trinidad. The alpha(3.7) globin gene deletion status was also studied with an observed gene frequency of 0.17. Among the 283 beta(S) chromosomes analyzed, the Benin haplotype was the most prevalent (61.8%) followed by Bantu (17.3%), Senegal (8.5%), Cameroon (3.5%), and Arab-Indian (3.2%), while 5.7% of them were atypical. This beta(S) haplotypes distribution differed from those previously described in other Caribbean islands (Jamaica, Guadeloupe, and Cuba), in agreement with the known involvement of the major colonial powers (Spain, France, and Great Britain) in the slave trade in Trinidad and documented an Indian origin of the beta(S) gene.
Databáze: OpenAIRE