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患者女18岁漯河人自幼左眼睑下垂,视物不清,多次在当地卫生院治疗,曾服中西药及局部滴眼无效,于1988年3月4日以上睑下垂收入院。患者父母非近亲结婚,其二姑双眼轻度下垂,家系其它成员无特殊眼病史。体格检查:发育正常,营养中等,心肺正常,右上腹轻度压疼,四肢及脊柱无异常。3月6日因上腹部阵发性疼行B超检查,诊断:肝左叶先天性缺损,先天性无胆囊,胆总管下段蛔虫症。脾、肾、胰均未见异常。
18-year-old female Luohe people from the left ptosis, blurred vision, many times in the local hospital for treatment, had served Chinese and Western medicine and local ineffective drip, in March 4, 1988 above the ptosis income hospital. The parents of the patients were married to non-relatives, their sons and daughters drooped slightly, and other members of the pedigree had no history of special eye disease. Physical examination: normal development, moderate nutrition, normal heart and lungs, mild right upper quadrant pain, limbs and spine without exception. March 6 due to paroxysmal abdominal pain in the upper abdomen B-line diagnosis, diagnosis: congenital defects of the left lobe of the liver, congenital absence of the gallbladder, common bile duct ascariasis. Spleen, kidney, pancreatic were no abnormalities.