肝豆状核变性又称wilson病,是一种常染色体隐性遗传的铜代谢障碍所引起的家族性疾病。临床表现为进行性加剧的肢体震颤、肌肉强直,构音困难,精神症状,肝硬化及角膜色素环等症状。国外统计发病占1/20万人,好发于10～15岁,男多于女,发病缓慢,早期确诊困难。现将我院2例报告如下:例1,患者女,38岁,农妇,主因四肢无 Wilson’s disease, also known as Wilson’s disease, is an autosomal recessive disorder caused by copper metabolism caused by a familial disease. Clinical manifestations of aggravating limb tremor, muscle rigidity, dysarthria, psychiatric symptoms, cirrhosis and corneal pigment ring and other symptoms. The incidence of foreign statistics 1/2 million, occurs in 10 to 15 years old, more men than women, the incidence is slow, early diagnosis difficult. Now in our hospital 2 cases are reported as follows: Example 1, female patient, 38 years old, peasant women, mainly due to limbs without