The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China

阵发性运动障碍 运动障碍 医学 先证者 儿科 遗传学 内科学 突变 生物 基因 疾病 帕金森病
作者
Xiao‐Jun Huang,Shi‐Ge Wang,Xia‐Nan Guo,Wotu Tian,Feixia Zhan,Zeyu Zhu,Xiao‐Meng Yin,Qing Liu,Kaili Yin,Xiao‐Rong Liu,Yu Zhang,Zhenguo Liu,Xiaoli Liu,Lan Zheng,Tian Wang,Li Wu,Tian‐Yi Rong,Yan Wang,Mei Zhang,Guang‐Hui Bi
出处
期刊:Movement Disorders [Wiley]
卷期号:35 (8): 1428-1437 被引量:42
标识
DOI:10.1002/mds.28061
摘要

BACKGROUND: Paroxysmal kinesigenic dyskinesia is a spectrum of involuntary dyskinetic disorders with high clinical and genetic heterogeneity. Mutations in proline-rich transmembrane protein 2 have been identified as the major pathogenic factor. OBJECTIVES: We analyzed 600 paroxysmal kinesigenic dyskinesia patients nationwide who were identified by the China Paroxysmal Dyskinesia Collaborative Group to summarize the clinical phenotypes and genetic features of paroxysmal kinesigenic dyskinesia in China and to provide new thoughts on diagnosis and therapy. METHODS: The China Paroxysmal Dyskinesia Collaborative Group was composed of departments of neurology from 22 hospitals. Clinical manifestations and proline-rich transmembrane protein 2 screening results were recorded using unified paroxysmal kinesigenic dyskinesia registration forms. Genotype-phenotype correlation analyses were conducted in patients with and without proline-rich transmembrane protein 2 mutations. High-knee exercises were applied in partial patients as a new diagnostic test to induce attacks. RESULTS: Kinesigenic triggers, male predilection, dystonic attacks, aura, complicated forms of paroxysmal kinesigenic dyskinesia, clustering in patients with family history, and dramatic responses to antiepileptic treatment were the prominent features in this multicenter study. Clinical analysis showed that proline-rich transmembrane protein 2 mutation carriers were prone to present at a younger age and have longer attack duration, bilateral limb involvement, choreic attacks, a complicated form of paroxysmal kinesigenic dyskinesia, family history, and more forms of dyskinesia. The new high-knee-exercise test efficiently induced attacks and could assist in diagnosis. CONCLUSIONS: We propose recommendations regarding diagnostic criteria for paroxysmal kinesigenic dyskinesia based on this large clinical study of paroxysmal kinesigenic dyskinesia. The findings offered some new insights into the diagnosis and treatment of paroxysmal kinesigenic dyskinesia and might help in building standardized paroxysmal kinesigenic dyskinesia clinical evaluations and therapies. © 2020 International Parkinson and Movement Disorder Society.
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