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遗传性口形红细胞增多症是一种红细胞膜异常的先天性溶血性贫血,其红细胞形态异常,属常染色体遗传。本病罕见,现将我们发现的一例并附电镜观察报告如下。临床资料患者,女,19岁,医学生。患者自幼有皮肤巩膜黄染,每逢过度疲劳及情绪紧张时,黄染加深,自觉疲乏、纳差,经休息症状可自行缓解,黄染也可减轻。曾查肝功能,除黄疸指数增高(22～28~u),凡登白反应双相外余均正常。祖辈世居上海,无疫
Hereditary Oral polycythemia is a congenital hemolytic anemia of abnormal erythrocyte membrane, the abnormal erythrocyte morphology, is an autosomal genetic. The disease is rare, we will find an example and attached to the electron microscopy report is as follows. Clinical data Patients, female, 19 years old, medical student. Patients with skin scleral yellow dye since childhood, whenever fatigue and emotional stress, yellow dye deepen, conscious fatigue, anorexia, the symptoms can be relieved by rest, yellow dye can also be reduced. Had checked liver function, in addition to jaundice index increased (22 ~ 28 ~ u), Van den Berg reaction outside the two-phase normal. Ancestors living in Shanghai, no disease