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遗传性球形细胞增多症是一种常染色体显性遗传性疾病。常因黄疸、脾肿大、贫血,腿部溃疡,胆石症等情况引起临床注意。国内报道已近百例。现将我们所遇一例报告如下: 张××,男,23岁,蒙古族,通辽县人,农民,住院号791637。因淋雨后发冷发热、黄疸、极度衰竭于1979年10月18日入院。患者平素健康状况欠佳,经常乏力、黄疸。曾
Hereditary spherocytosis is an autosomal dominant genetic disorder. Often due to jaundice, splenomegaly, anemia, leg ulcers, cholelithiasis and other conditions caused by clinical attention. Nearly 100 cases reported in the country. Now we have a case of a report as follows: Zhang × ×, male, 23 years old, Mongolian, Tongliao County, peasant, hospital number 791637. Due to cold after the rain fever, jaundice, extreme failure in October 18, 1979 admission. Patients generally poor health, often fatigue, jaundice. Once