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作 者:Xiaojuan Tian Changhong Ding Ming Liu Lifang Dai Zixing Xie Tie Fang
机构地区:[1]Department of Neurology,Neurological Center,Beijing Children’s Hospital,Capital Medical University,National Center For Children’s Health,Beijing,China [2]Department of Functional Neurosurgery,Neurological Center,Beijing Children’s Hospital,Capital Medical University,National Center For Children’s Health,Beijing,China
出 处:《Pediatric Investigation》2024年第2期154-156,共3页儿科学研究(英文)
基 金:supported by the China Association Against Epilepsy Scientific Research Project(CU-2022-018).
摘 要:To the editor:Myoclonus-dystonia syndrome(MDS)(OMIM15990)is a heritable disorder characterized by early onset subcortical myoclonic jerks and/or less prominent dystonia.This leads to disability and is often refractory to medical treatment.1 Deep brain stimulation(DBS)for the treatment of refractory MDS has been proven effective in adults for reducing both myoclonic jerks and dystonia.1,2,3 Here,we describe the application of bilateral globus pallidus internus(GPi)DBS in a 5-year-old boy diagnosed with MDS.
分 类 号:R748[医药卫生—神经病学与精神病学]
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