Ghosh K, Chakrabarty A K, Mohanty D, Das K C
Trop Geogr Med. 1983 Sep;35(3):267-71.
Eight cases of haemoglobin E-beta.thalassaemia are described. Seven of them are natives of Punjab, a Northwest province of India, and one is a native of Rajasthan, a province adjacent to Punjab. Hb E is rarely encountered in Punjab, but beta-thalassaemia is relatively common. The interaction of Hb E with beta-thalassaemia resulted in a varying severity of phenotypic manifestations. An extraordinary feature in 3 out of 8 cases was the presence of a high percentage of Hb E (94 to 96%) and proportionately low Hb F (4 to 6%). The interacting thalassaemia in 5 patients was of beta0 type and in 3 patients of beta+ type.
本文描述了8例血红蛋白E-β地中海贫血病例。其中7例来自印度西北部的旁遮普邦,1例来自与旁遮普邦相邻的拉贾斯坦邦。在旁遮普邦,血红蛋白E很少见,但β地中海贫血相对常见。血红蛋白E与β地中海贫血的相互作用导致了不同严重程度的表型表现。8例中有3例的一个特殊特征是血红蛋白E的百分比很高(94%至96%),而血红蛋白F的比例相应较低(4%至6%)。5例患者的相互作用性地中海贫血为β0型,3例为β+型。