论文部分内容阅读
本病虽不罕见,但每易误诊。我们于1978年收治同一家族中发病2例,并作了三代11人的调查。报道如下: 一、病例介绍例1 女,32岁,住院号5793,因头晕、乏力、皮肤黄染32年、近4个月加重,于1978年10月3日入院。患者自出生后即有皮肤黄染、无呕吐、发热、出血征,1月后黄疸呈持续不退,因肝脾肿大曾在某院诊断为“肝炎”,用保肝药或中药治疗,黄疸时轻时重,食欲尚可,无灰白色便,有牙龈、鼻腔
Although the disease is not uncommon, but each misdiagnosis. In 1978, we treated 2 patients with the same family and made a survey of 11 people in three generations. Reported as follows: First, the case introduced Example 1 female, 32 years old, hospital number 5793, due to dizziness, fatigue, skin yellow dye 32 years, nearly 4 months to aggravate, on October 3, 1978 admitted. Patients since the birth of skin yellow dye, no vomiting, fever, bleeding sign, jaundice was persistent after January, due to hepatosplenomegaly in a hospital diagnosed as “hepatitis”, with liver medicine or traditional Chinese medicine treatment, Jaundice when light weight, appetite is acceptable, no gray will be, with gums, nasal cavity