Department of Neurology, Division of Child Neurology, Louisiana State University Health Sciences Center at New Orleans, Children's Hospital, 200 Henry Clay Ave., New Orleans, LA, 70118, USA.
Neurotherapeutics. 2020 Oct;17(4):1713-1723. doi: 10.1007/s13311-020-00984-6. Epub 2021 Jan 6.
Pediatric movement disorders (PMDs) consist of a heterogeneous group of signs and symptoms caused by numerous neurological diseases. Different neurological disorders in children also share overlapping movement disorders making a diagnosis of the underlying cause of the movement disorder challenging. The similarity of the symptoms across multiple disease types suggests that there may be a final common motor pathway causing the overlapping movement disorders. There are numerous disorders in children associated with disturbances in tone and involuntary movements. This chapter will focus primarily on those disorders that involve abnormalities of tone and other important considerations of pediatric movement disorders. This chapter will address rating scales and goals for treatment and will include a review of symptomatic treatment and, where possible, the treatment of the underlying disease processes. The chapter will review representative disorders, including an inborn error of metabolism, an autoimmune disorder, and a group of neurodegenerative disorders. These examples demonstrate how the disorder's underlying pathophysiology results in a specific approach to the underlying disease and the associated conditions of tone and involuntary movements. Finally, the multiple treatment options for cerebral palsy and considerations of cerebral palsy mimics will be discussed.
儿科运动障碍(PMD)由多种神经系统疾病引起的一组异质性体征和症状组成。儿童的不同神经系统疾病也有重叠的运动障碍,这使得运动障碍的根本病因的诊断具有挑战性。多种疾病类型的症状相似,表明可能存在导致重叠运动障碍的最终共同运动通路。有许多与肌张力和不自主运动障碍相关的儿童疾病。本章将主要关注那些涉及肌张力异常和儿科运动障碍其他重要考虑因素的疾病。本章将讨论评定量表和治疗目标,并包括症状治疗的回顾,以及在可能的情况下,对潜在疾病过程的治疗。本章将回顾代表性疾病,包括先天性代谢缺陷、自身免疫性疾病和一组神经退行性疾病。这些例子说明了疾病的潜在病理生理学如何导致对潜在疾病以及相关的肌张力和不自主运动状况的特定治疗方法。最后,将讨论脑瘫的多种治疗选择和脑瘫模仿的考虑因素。