Wilosn综合征又称肝豆状核变性综合征，是一种常染色体隐性遗传性疾病，发病率约为1：30000，而因口腔病就诊者更为罕见，现将近年来我们遇到的2例介绍如下。1临床病例2例患者为男性，年龄分别为22岁、27岁。均因上肢和头颈区肌肉震颤、强直性运动受限，发音吞咽困难，分别在某 Wilosn syndrome, also known as hepatolenticular degeneration syndrome, is an autosomal recessive genetic disease, the incidence rate of about 1: 30000, while the patients with oral disease is more rare, now we have encountered in recent years 2 Examples are as follows. 1 Clinical cases 2 patients were male, aged 22 years, 27 years old. Both due to upper extremity and head and neck muscle tremor, tetany limited exercise, dysphagia, respectively, in a