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肝豆状核变性属常染色体隐性遗传性铜代谢障碍引起的疾病。为提高对本病的认识,现将1986年9月~1987年8月收治的2例报告如下。例1 男,14岁。以纳差、皮肤黄染一月,腹水、黑便半月于1986年9月收入院。一月前无明原因出现纳差、面黄、尿黄、乏力。曾在当地医院按肝炎治疗,症状逐日加重。半月前出现腹水及柏油便。既往无肝炎病史。父母非近亲结婚,体健,无肝炎史。体检:皮肤巩
Wilson’s disease is an autosomal recessive inherited copper metabolism disorders caused by the disease. To improve awareness of the disease, now in September 1986 ~ August 1987 admitted 2 cases are as follows. Example 1 male, 14 years old. With anorexia, skin yellow dye January, ascites, melena half month in September 1986 income hospital. A month ago no reason for anorexia, face yellow, yellow urine, fatigue. Hepatitis treatment in local hospitals, the symptoms increased day by day. Ascites and tar will appear half a month ago. No past history of hepatitis. Parents of non-relatives married, healthy, no history of hepatitis. Physical examination: skin Gong