论文部分内容阅读
肝豆状核变性又称wilson病,于1912年由Samuela A.K.Wilson首先系统详细描述,是一种遗传性铜代谢障碍所致的肝硬化和以基底节为主的脑部变性疾病。临床特点为进行性加重的锥体外系症状、精神症状、肝硬化、肾功能损害
Wilson’s disease, also known as Wilson’s disease, was first systematically described by Samuela A.K. Wilson in 1912 as a systemically inherited disorder of liver cirrhosis and basal ganglia degenerative disorders caused by hereditary copper metabolism disorders. Clinical features of progressive extrapyramidal symptoms, psychiatric symptoms, cirrhosis, impaired renal function