中国发作性运动诱发性运动障碍诊治指南  

Chinese guidelines for diagnosis and treatment of paroxysmal kinesigenic dyskinesia

作　　者：中华医学会神经病学分会神经遗传学组 中国医师协会神经内科医师分会神经遗传学组 吴志英[2] 王柠[3] 曹立 唐北沙 Chinese Society of Neurogenetics;Neurogenetics Group of Neurology Branch of Chinese Medical Doctor Association;Wu Zhiying;Wang Ning(不详;Department of Neurology,Second Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou 310009,China;Department of Neurology,First Affiliated Hospital of Fujian Medical University,Fuzhou 350005,China)

机构地区：[1]不详 [2]浙江大学医学院附属第二医院神经内科,杭州310009 [3]福建医科大学附属第一医院神经内科,福州350005 [4]上海交通大学附属第六人民医院 [5]中南大学湘雅医院

出　　处：《中华神经科杂志》2022年第1期9-14,共6页Chinese Journal of Neurology

摘　　要：发作性运动诱发性运动障碍(PKD)是发作性运动障碍中最常见的类型,以突然运动诱发短暂的不自主运动为特征。由于相对少见,PKD易被误诊为癫痫或其他发作性疾病。为提高临床医生对该病的认识及规范化诊治,我国PKD诊治领域的专家反复讨论撰写了该指南,并在神经遗传学组会议上反复讨论修改后定稿。内容包括PKD的临床表现、诊断、鉴别诊断、治疗及遗传咨询。Paroxysmal kinesigenic dyskinesia(PKD)is the most common type of paroxysmal dyskinesia,characterized by involuntary movements which are usually precipitated by sudden movement.Because of its relative rarity,PKD is easily misdiagnosed as epilepsy or other paroxysmal disorders.In order to improve clinicians′understanding and standardize the diagnosis and treatment of this disease,experts in the field of PKD in China repeatedly discussed and wrote the guidelines,which were finalized after repeated discussions and revisions at the meeting of Chinese Society of Neurogenetics and Neurogenetics Group of Neurology Branch of Chinese Medical Doctor Association.The contents include clinical manifestations,diagnosis and differential diagnosis,treatment and genetic counseling of PKD.

关 键 词：发作性运动诱发性运动障碍 诊断 治疗 指南 

分 类 号：R741[医药卫生—神经病学与精神病学]