遗传性球形红细胞增多症是比较少见的疾病。主要是红细胞膜结构异常,常于生后短时间内发生溶血性黄疸,可造成核黄疸。现将我院发现的1例报告如下: 患者,男,出生20小时,主因皮肤黄染16小时于1988年1月1日11时由妇产科转入我科。患儿宫内孕40周,20小时前经 Hereditary spherocytosis is a relatively rare disease. Mainly abnormal erythrocyte membrane structure, often occurring in a short period of time after hemolytic jaundice, can cause nuclear jaundice. A case report found in our hospital are as follows: Patients, male, born 20 hours, mainly due to skin yellow dye 16 hours at 1 o’clock on January 1, 1988 from obstetrics and gynecology into our department. Children with intrauterine pregnancy 40 weeks, 20 hours before