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Stereotypic Movement Disorders

机译:陈规定型运动障碍

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This review summarizes motor stereotypies in terms of description, prevalence, pathophysiology, diagnosis and management. They are fixed and persistent movements. Stereotypies begin before 3 years of age and continue into adulthood. Primary motor stereotypies occur in children of normal intelligence, whereas secondary stereotypies ensue in the setting of an additional diagnosis such as autism spectrum disorder or other neurologic disorders. They are highly associated with comorbidities such as anxiety, obsessive-compulsive symptoms, inattention, and tics. The pathophysiology of stereotypies involves fronto-striatal overactive dopaminergic pathways, and underactive cholinergic and GABAergic inhibitory pathways. No genetic markers have been identified despite a clear genetic predisposition. Behavioral therapy is the principle treatment. Future studies will focus on identifying genetic markers, and on better understanding the functional and structural neurobiology of these movements.
机译:本综述总结了在描述,患病率,病理生理学,诊断和管理方面的运动态度型。 它们是固定的和持续运动。 刻板型在3岁之前开始,继续进入成年期。 初级运动刻板型在正常智能的儿童中出现,而次要刻板型在额外的诊断中随之而来,例如自闭症谱系障碍或其他神经系统。 它们与焦虑,强迫性症状,疏忽和抽搐等合并症高度相关。 陈规定型的病理生理学涉及前纹脊髓侧面活性多巴胺能途径,含有胆碱能和巨石能抑制途径。 尽管遗传易感性仍未鉴定出遗传标记。 行为治疗是原理治疗。 未来的研究将重点关注识别遗传标记,并更好地了解这些运动的功能和结构神经生物学。

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