首页> 外文期刊>Acta Haematologica >Molecular Heterogeneity of Thalassemia among Pregnant Laotian Women
【24h】

Molecular Heterogeneity of Thalassemia among Pregnant Laotian Women

机译:老挝孕妇地中海贫血的分子异质性

获取原文
获取原文并翻译 | 示例
           

摘要

Background and Aims:A pilot screening program for thalassemia was initiated in the Lao People's Democratic Republic. This study aimed to describe the genotype diversity and hematologic features of thalassemia among the participating pregnant women. Methods: Blood samples of 411 pregnant Laotian women were collected. Hemoglobin (Hb) profiles were determined using a capillary zone electrophoresis system. Mutations of alpha- and beta-globin genes were investigated using a polymerase chain reaction and related techniques. Results: As many as 26 different thalassemia genotypes including non-transfusion-dependent thalassemia, i.e. Hb E-beta-thalassemia, Hb H, and EA Bart's diseases, were identified. A variety of phenotypic expressions of hematologic features and Hb profiles were observed, including an unusual phenotype of Hb E-beta(0) thalassemia with 89.1% Hb E, 1.6% Hb F, and 9.3% Hb A(2). Conclusions: The remarkable genotype-phenotype diversity indicates a need for careful laboratory interpretation in order to provide appropriate genetic counseling and care to the Laotian population. (c) 2015 S. Karger AG, Basel
机译:背景与目的:在老挝人民民主共和国启动了地中海贫血筛查试验计划。本研究旨在描述参与孕妇地中海贫血的基因型多样性和血液学特征。方法:收集411名老挝孕妇的血液样本。使用毛细管区带电泳系统确定血红蛋白(Hb)分布。使用聚合酶链反应和相关技术研究了α-珠蛋白和β-珠蛋白基因的突变。结果:鉴定出多达26种不同的地中海贫血基因型,包括非输血依赖性地中海贫血,即HbE-β地中海贫血,Hb H和EA Bart病。观察到了多种血液学特征和血红蛋白特征的表型表达,包括具有89.1%血红蛋白E,1.6%血红蛋白F和9.3%血红蛋白A(2)的Hb E-beta(0)地中海贫血的异常表型。结论:显着的基因型-表型多样性表明需要仔细的实验​​室解释,以便为老挝人口提供适当的遗传咨询和护理。 (c)2015 S.Karger AG,巴塞尔

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号