论文部分内容阅读
血红蛋白 E 复合β地中海贫血(以下简称 HbE-β地贫),属遗传性溶血性贫血,Itano 和 Na-Nakorn 等先后报道了 HbE 和 HbE-β地贫,此病在我国较为少见,在长江以北更属罕见,我院收治1例祖孙三代世居河北省的 HbE-β地贫,报道如下。
Hemoglobin E complex beta thalassemia (hereinafter referred to as HbE-beta thalassemia), is a hereditary hemolytic anemia, Itano and Na-Nakorn have reported HbE and HbE-beta thalassemia, the disease is rare in our country, in the Yangtze River to North is even more rare, our hospital admitted to a case of three generations of Habitat Hebei HbE-β thalassemia, reported as follows.