论文部分内容阅读
Huntington舞蹈病是以舞蹈动作与进行性痴呆为特点的中枢神经系统变性病,多为成年发病,常染色体显性遗传。于1980年我们曾报告2例,其后又遇3例,现报告如下,并作简要讨论。例1,男,34岁,工人,已婚。自1973年起怀疑妻与他人关系密切,便日夜跟踪其妻,当目击妻与男性交谈或接近,便出言不逊,逼妻不敢与男性交往。否认自己有病。诊断精神分裂症,经抗精神病药物治疗无效,且日益加重。于1978年夏其子淹死,便沉默不语,彻夜不眠,渐出现全身不自主运动。先表现为挤眉呶嘴,皱额,渐及四肢不自主的伸屈,旋转,耸肩,挺胸,摆臀,扭躯。
Huntington chorea is a central nervous system degenerative disease characterized by choreography and progressive dementia, mostly adult onset and autosomal dominant inheritance. In 1980, we reported 2 cases and then 3 cases. We report the following and give a brief discussion. Example 1, male, 34 years old, worker, married. Since 1973, his wife suspected of being close to others, they will follow his wife day and night, when witnessing the wife to talk with or close to men, they retributive, forced the wife did not dare to deal with men. Deny yourself sick. Diagnosis of schizophrenia, antipsychotic treatment ineffective, and increasing. In the summer of 1978, his son drowned, he was silent, sleepless nights, gradually involuntary movement of the body. The first performance of squeeze Meizuizui, wrinkles, gradually involuntary flexion and extension of the limbs, rotation, shrugging, chest, hip, torsion torsion.