Literature DB >> 10975441

Sickle cell anemia and beta-globin gene cluster haplotypes in Colombia.

F Cuéllar-Ambrosi1, M C Mondragón, M Figueroa, C Préhu, F Galactéros, A Ruiz-Linares.   

Abstract

We studied 46 unrelated sickle cell anemia patients from the western region of Colombia which has the largest Black population of the country. Twenty-three children and 23 adults were studied. The distribution of haplotypes in the children was 58% Bantu, 38% Benin, and 4% Senegal, and in the adults it was 59.4% Bantu, 35.1% Benin, and 5.5% Senegal (p = 0.920). All 92 chromosomes had typical African haplotypes, Bantu 55.5%, Benin 34.8%, Senegal, 4.3%, and Cameroon, 5.4%. Our results suggest a lack of differential survival among patients with sickle cell anemia and typical beta-globin gene cluster haplotypes. They also agree closely with historical data that indicate that most African slaves brought to Colombia originated from Angola (Bantu population) and the Sao Thomó Island in the Bight of Benin (Central West Africa).

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Year:  2000        PMID: 10975441     DOI: 10.3109/03630260008997529

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  2 in total

1.  Etiology and Viral Genotype in Patients with End-Stage Liver Diseases admitted to a Hepatology Unit in Colombia.

Authors:  Fabian Cortes-Mancera; Carmen Luisa Loureiro; Sergio Hoyos; Juan-Carlos Restrepo; Gonzalo Correa; Sergio Jaramillo; Helene Norder; Flor Helene Pujol; Maria-Cristina Navas
Journal:  Hepat Res Treat       Date:  2011-09-20

2.  Frequency and origin of haplotypes associated with the beta-globin gene cluster in individuals with trait and sickle cell anemia in the Atlantic and Pacific coastal regions of Colombia.

Authors:  Cristian Fong; María Alejandra Lizarralde-Iragorri; Diana Rojas-Gallardo; Guillermo Barreto
Journal:  Genet Mol Biol       Date:  2013-11-08       Impact factor: 1.771

  2 in total

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