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两个加拿大家庭中一种新型55.1 kb(G)γ((A)γδβ)0-地中海贫血缺失的分子特征分析

Molecular characterization of a novel 55.1 kb (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion in two Canadian families.

作者信息

Voruganti Indu, Eng Barry, Waye John S

机构信息

Molecular Diagnostic Genetics, Hamilton Regional Laboratory Medicine Program, Hamilton, ON, Canada.

出版信息

Hemoglobin. 2009;33(6):422-7. doi: 10.3109/03630260903333088.

Abstract

We report two Canadian families in which there are four carriers of a novel (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion. The patients all have mild microcytosis and hypochromia, and elevated levels of Hb F ranging from 9.7 to 17.3%. The precise endpoints of the deletion have been identified and are unique relative to other forms of (G)gamma((A)gammadeltabeta)(0)-thal reported in the literature. The deletion encompasses approximately 55.1 kb, beginning approximately 1.6 kb downstream of the (G)gamma-globin gene and extending approximately 29.0 kb downstream of the beta-globin gene.

摘要

我们报告了两个加拿大家庭,其中有四名新型(G)γ(A)γδβ(0)-地中海贫血缺失的携带者。患者均有轻度小红细胞症和低色素血症,Hb F水平升高,范围为9.7%至17.3%。已确定该缺失的精确端点,相对于文献中报道的其他形式的(G)γ(A)γδβ(0)-地中海贫血而言是独特的。该缺失约为55.1 kb,始于(G)γ-珠蛋白基因下游约1.6 kb处,并延伸至β-珠蛋白基因下游约29.0 kb处。

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