Eyelid dysfunction in neurodegenerative, neurogenetic, and neurometabolic disease

46Citations
Citations of this article
64Readers
Mendeley users who have this article in their library.

Abstract

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 1).

Cite

CITATION STYLE

APA

Hamedani, A. G., & Gold, D. R. (2017, July 18). Eyelid dysfunction in neurodegenerative, neurogenetic, and neurometabolic disease. Frontiers in Neurology. Frontiers Media S.A. https://doi.org/10.3389/fneur.2017.00329

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free