血红蛋白病
单倍型
珠蛋白
遗传学
地中海贫血
生物
基因型
溶血性贫血
基因
免疫学
作者
Luis Felipe Guzmán,Francisco J. Perea,Marı́a Teresa Magaña,Karina R. Morales-González,M. Luz Chávez-Velazco,B Ibarra
出处
期刊:Hemoglobin
[Informa]
日期:2010-11-15
卷期号:34 (6): 509-515
被引量:2
标识
DOI:10.3109/03630269.2010.526483
摘要
Between 1978 and 2009, we studied 1,863 Mexican Mestizo patients with clinical data compatible with a hemoglobinopathy. Of these patients, 382 had some hemoglobin (Hb) abnormality (20.5%), 128 had a sickle cell hemoglobinopathy, representing a general frequency of 6.9%, which is similar to the percentage observed in previous studies on Mexican Mestizos. We analyzed the 5' β-globin haplotype (5'Hp) in 79 unrelated β(S) chromosomes (26 β(S)/β(S), 14 β(S)/β(Thal), nine β(S)/β(A) and four β(S)/β(D)), and four haplotypes were observed: 72.2% CAR 24.1% Benin, 2.5% Senegal and 1.2% Cameroon; the last two are reported for first time in Mexico. In some Latin American populations such as Brazil, the Bantu haplotype predominates, while in others such as Jamaica, the Benin haplotype is the most frequent, showing heterogeneity of African genes as a consequence of different regions involved in the slave trade.
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