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Hemoglobin ; 38(5): 316-8, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25271992

RESUMO

The aim of this study was the determination of hemoglobin (Hb) variants and ABO blood groups in a school population aged 6 to 9 years in the township of Agbandé-Yaka in North Togo. A cross-sectional study was carried out on 570 children of four primary schools at Agbande-Yaka, between March and July 2010. Hemoglobin characterization was done by alkaline buffer electrophoresis and the blood types ABO-Rhesus (Rh) D by immuno-hematological methods. A Hb variant was detected in 37.0% of the schoolchildren. Among them, the AS trait accounted for 11.9% and the AC trait for 20.2%. Homozygous Hb S (HBB: c.20A>T) was not found but Hb C (HBB: c.19G>A) appeared at a frequency of 3.3%, while compound heterozygotes carrying Hb SC were seen at a frequency of 1.6%. The O, B and A blood groups accounted for 49.0, 26.8 and 21.9%, respectively. The Hb anomalies reached a high prevalence in this school population. These results are remarkable by the absence of homozygous Hb S individuals compared to homozygous Hb C individuals, which were as numerous as expected. The frequencies of the ABO blood groups are similar to what has been found in other West African populations.


Assuntos
Sistema ABO de Grupos Sanguíneos/sangue , Doença da Hemoglobina C/epidemiologia , Hemoglobina C/análise , Doença da Hemoglobina SC/epidemiologia , Hemoglobina Falciforme/análise , Polimorfismo de Nucleotídeo Único , Sistema do Grupo Sanguíneo Rh-Hr/sangue , Alelos , Criança , Estudos Transversais , Feminino , Frequência do Gene , Hemoglobina C/genética , Doença da Hemoglobina C/sangue , Doença da Hemoglobina C/genética , Doença da Hemoglobina SC/sangue , Doença da Hemoglobina SC/genética , Hemoglobina Falciforme/genética , Heterozigoto , Homozigoto , Humanos , Masculino , Programas de Rastreamento , Prevalência , Instituições Acadêmicas , Togo/epidemiologia
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