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6—磷酸葡萄糖脱氢酶缺陷(G-6-PD)缺乏是一种伴性不完全显性遗传性溶血性疾病,在我国华南地区,尤其是广东,相当多见。而阵发性睡眠性血红蛋白尿(PNH),是一种获得性红细胞膜异常的溶血性疾患,是一个少见疾病。G-6-PD缺陷合并PNH国内外罕见,我室曾收治一例现报告如下: 患者(住院号4649)男性,26岁,广东籍,工人。于1981年开始无明显诱因反复牙龈出血,先后两次在某医院住院。经检查诊为G-6-PD缺乏。1982年因症状反复发作第3次住
Lack of 6-phosphoglucose dehydrogenase deficiency (G-6-PD) is a complication of incomplete dominant hereditary hemolytic disease, in southern China, especially Guangdong, quite common. And paroxysmal nocturnal hemoglobinuria (PNH), is a hemolytic disorder of acquired erythrocyte abnormalities, is a rare disease. G-6-PD defects combined with PNH rare at home and abroad, my room was admitted to a case report is as follows: Patients (hospital number 4649) Male, 26 years old, Guangdong nationality, workers. In 1981 there was no obvious incentive to repeated bleeding gums, has twice in a hospital. The examination revealed G-6-PD deficiency. Repeated symptoms for the third time in 1982 lived