Antisaccade Deficits in Stiff Person Syndrome

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Identifier 20170402_nanos_posters_102
Title Antisaccade Deficits in Stiff Person Syndrome
Creator Amrita Singh; Wangzikang Zhang; Jeffrey Odel; Michael Goldberg; Linus Sun
Affiliation (AS) (WZ) (JO) (MG) (LS) Columbia University, New York, New York
Subject Paraneoplastic Syndromes; Higher Visual Cortical Functions; Ocular Motility; Neuro-ophth & Systyemic Disease; Nystagmus
Description The antisaccade task is a clinically useful sign of frontal cortical dysfunction (Hallet,1978). In this task, subjects must make a saccade away from a salient stimulus to a spatial location reflected 180° away. Normal subjects make about 10% errors in this task, but frontal patients make many more. Stiff Person Syndrome (SPS) is a disorder characterized by muscle rigidity, spasm, and ataxia, in which 85% of patients have antibodies against glutamic acid decarboxylase (GAD) an enzyme necessary for GABA synthesis. Previous studies of these patients have identified oculomotor abnormalities, including esotropia (Economides, 2005), multi-component and slow vertical saccades, decreased smooth pursuit gain, downbeat nystagmus (Ances, 2005), and ophthalmoplegia (Pittock, 2006).
Date 2017
Language eng
Format application/pdf
Type Text
Source 2017 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS 2017: Poster Presentations
Collection Neuro-Ophthalmology Virtual Education Library: NANOS Annual Meeting Collection: https://novel.utah.edu/collection/nanos-annual-meeting-collection/
Publisher North American Neuro-Ophthalmology Society
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah
Rights Management Copyright 2017. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6n62fgw
Setname ehsl_novel_nam
ID 1272622
Reference URL https://collections.lib.utah.edu/ark:/87278/s6n62fgw
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