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Eyelid Dysfunction in Neurodegenerative Neurogenetic and Neurometabolic Disease

机译:神经变性神经遗传和神经代谢疾病中的眼睑功能障碍

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摘要

Eye movement abnormalities are among the earliest clinical manifestations of inherited and acquired neurodegenerative diseases and play an integral role in their diagnosis. Eyelid movement is neuroanatomically linked to eye movement, and thus eyelid dysfunction can also be a distinguishing feature of neurodegenerative disease and complements eye movement abnormalities in helping us to understand their pathophysiology. In this review, we summarize the various eyelid abnormalities that can occur in neurodegenerative, neurogenetic, and neurometabolic diseases. We discuss eyelid disorders, such as ptosis, eyelid retraction, abnormal spontaneous and reflexive blinking, blepharospasm, and eyelid apraxia in the context of the neuroanatomic pathways that are affected. We also review the literature regarding the prevalence of eyelid abnormalities in different neurologic diseases as well as treatment strategies (Table ).>Table 1Summary of eyelid disorder mechanisms, associations, and treatments in neurodegenerative and neurogenetic disease.
机译:眼球运动异常是遗传性和后天性神经退行性疾病的最早临床表现之一,并且在其诊断中起着不可或缺的作用。眼睑运动在神经解剖学上与眼球运动有关,因此眼睑功能障碍也可以是神经退行性疾病的显着特征,并且可以补充眼球运动异常,以帮助我们了解其病理生理。在这篇综述中,我们总结了神经变性,神经遗传和神经代谢疾病中可能发生的各种眼睑异常。我们讨论了眼睑疾病,例如上睑下垂,眼睑后缩,自发和自发性眨眼异常,睑裂,眼睑失用症,以及受影响的神经解剖学途径。我们还回顾了有关不同神经系统疾病眼睑异常的患病率以及治疗策略的文献(表)。<!-table ft1-> <!-table-wrap mode =“ anchored” t5-> < h3>表1 <!-标题a7->神经退行性疾病和神经遗传疾病的眼睑疾病机制,关联和治疗的概述。

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