A silent composite hemoglobinopathy characterized by gene sequencing.

A Zorai, I Moumni, I Benmansour, D Chaouachi, A Ghanem, S Abbes
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Abstract

We report the case of a 35-year-old Tunisian women with a chronic anemia non investigated for a long time. Laboratory analysis using advanced technology of DNA sequencing revealed a compound heterozygote for Hb O Arab and cd 39 beta degrees-thalassemia. It's the first time that such a genotype has been characterized by gene sequencing.

一种以基因测序为特征的隐性复合血红蛋白病。
我们报告的情况下,35岁的突尼斯妇女慢性贫血未调查了很长一段时间。利用先进的DNA测序技术进行实验室分析,发现一种阿拉伯血红蛋白和cd39 β度的复合杂合子-地中海贫血。这是第一次通过基因测序来表征这种基因型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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