El-Hazmi M A, Lehmann H
Acta Haematol. 1980;63(5):268-73. doi: 10.1159/000207414.
In the Arabian peninsula, haemoglobinopathies, though very interesting, are still far from being fairly established. With the exception of the eastern province of Saudi Arabia, where several aspects of the sickle-cell disease have been focused upon, few reports have appeared in the literature. However, in 1974 one of us (M.A.F. E.H.) has initiated a comprehensive investigation in collaboration with the Ministry of Health on haemoglobinopathies in various parts of the country. These studies have revealed a new pocket for the sickle-cell gene and a new structural abnormality. In the present report we describe the first finding of Hb O Arab in Saudi Arabia, which may shed more light on the anthropological significance of this haemoglobin variant.
在阿拉伯半岛,血红蛋白病虽然非常有趣,但仍远未得到充分确立。除了沙特阿拉伯东部省份,那里对镰状细胞病的几个方面进行了重点研究外,文献中很少有相关报道。然而,1974年,我们中的一人(M.A.F. E.H.)与卫生部合作,在该国各地启动了一项关于血红蛋白病的全面调查。这些研究发现了镰状细胞基因的一个新聚集区和一种新的结构异常。在本报告中,我们描述了在沙特阿拉伯首次发现的Hb O Arab,这可能会为这种血红蛋白变体的人类学意义提供更多线索。