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儿童先天性代谢缺陷及运动障碍。

Inborn errors of metabolism and motor disturbances in children.

机构信息

Neurology and Metabolism Department, Hospital Sant Joan de Déu, 08950 Esplugues, Barcelona, Spain.

出版信息

J Inherit Metab Dis. 2009 Oct;32(5):618-29. doi: 10.1007/s10545-009-1194-9.

Abstract

Motor disturbances are very common in paediatric neurology. Often families can be reassured that these are just variants of normal development. However, abnormal movements can also be the hallmark of severe brain dysfunction of different and complex origins. This review concentrates on motor disturbances as frequent and important symptoms of inborn errors of metabolism. A structured diagnostic approach is developed taking into account age-dependent physiological developments and pathophysiological responses of gross and fine motor functions. A series of investigations are presented with the primary aim of early diagnosis of treatable conditions. The correct recognition and differentiation of movement disorders (ataxia, rigid akinetic syndrome (Fparkinsonism_), dystonia, athetosis, tremor,and others), spasticity, and neuromuscular disorders, requires profound neurological expertise. A high level of suspicion and close interaction between paediatric neurologists and specialists in inborn errors of metabolism are indispensable to effectively and timely identify patients in whom motor disturbances are the presenting and/or main symptom of an inborn error.

摘要

运动障碍在儿科神经病学中非常常见。通常情况下,家属会得到安慰,这些只是正常发育的变异。然而,异常运动也可能是不同且复杂起源的严重脑功能障碍的标志。本篇综述集中讨论运动障碍,因为其是代谢性遗传病的常见且重要的症状。在考虑年龄相关的生理发育和粗、细运动功能的病理生理反应的基础上,制定了一种结构化的诊断方法。提出了一系列检查,主要目的是早期诊断可治疗的疾病。正确识别和区分运动障碍(共济失调、僵硬运动不能综合征(类帕金森病)、肌张力障碍、舞蹈病、震颤等)、痉挛和神经肌肉疾病,需要深厚的神经学专业知识。儿科神经病学家和代谢性遗传病专家之间高度怀疑和密切互动是必不可少的,以有效地、及时地识别出以运动障碍为主要表现或主要症状的患者,这些患者患有代谢性遗传病。

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