Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Hemoglobin ; 38(5): 316-8, 2014.
Article in English | MEDLINE | ID: mdl-25271992

ABSTRACT

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.


Subject(s)
ABO Blood-Group System/blood , Hemoglobin C Disease/epidemiology , Hemoglobin C/analysis , Hemoglobin SC Disease/epidemiology , Hemoglobin, Sickle/analysis , Polymorphism, Single Nucleotide , Rh-Hr Blood-Group System/blood , Alleles , Child , Cross-Sectional Studies , Female , Gene Frequency , Hemoglobin C/genetics , Hemoglobin C Disease/blood , Hemoglobin C Disease/genetics , Hemoglobin SC Disease/blood , Hemoglobin SC Disease/genetics , Hemoglobin, Sickle/genetics , Heterozygote , Homozygote , Humans , Male , Mass Screening , Prevalence , Schools , Togo/epidemiology
SELECTION OF CITATIONS
SEARCH DETAIL
...