Saccade dysmetria in Williams–Beuren syndrome

Numerous studies have described the poor visuo-spatial processing capacities of subjects with Williams–Beuren syndrome (WBS), a genetically based developmental disorder. Since visual perception and eye movements are closely related we hypothesized that the poor visuo-spatial processing capacities of...

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Published inNeuropsychologia Vol. 42; no. 5; pp. 569 - 576
Main Authors van der Geest, J.N., Lagers-van Haselen, G.C., van Hagen, J.M., Govaerts, L.C.P., de Coo, I.F.M., de Zeeuw, C.I., Frens, M.A.
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 2004
Elsevier Science
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ISSN0028-3932
1873-3514
DOI10.1016/j.neuropsychologia.2003.11.003

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Abstract Numerous studies have described the poor visuo-spatial processing capacities of subjects with Williams–Beuren syndrome (WBS), a genetically based developmental disorder. Since visual perception and eye movements are closely related we hypothesized that the poor visuo-spatial processing capacities of subjects with WBS might be related to a poor saccadic control. Thereto, we recorded horizontal and vertical saccadic eye movements to targets using infrared video-oculography in 27 subjects with WBS and eight healthy controls. In the WBS group saccadic gains were highly variable, both between and within individual subjects, and they often needed more than one correction saccade to reach the target. Ten (out of a subgroup of 22) WBS subjects showed a large number of hypometric and/or hypermetric saccades, and, also a left–right asymmetry in saccadic gains was observed in WBS. We conclude that the observed impairments in saccadic control are likely to affect the proper processing of visuo-spatial information.
AbstractList Numerous studies have described the poor visuo-spatial processing capacities of subjects with Williams-Beuren syndrome (WBS), a genetically based developmental disorder. Since visual perception and eye movements are closely related we hypothesized that the poor visuo-spatial processing capacities of subjects with WBS might be related to a poor saccadic control. Thereto, we recorded horizontal and vertical saccadic eye movements to targets using infrared video-oculography in 27 subjects with WBS and eight healthy controls. In the WBS group saccadic gains were highly variable, both between and within individual subjects, and they often needed more than one correction saccade to reach the target. Ten (out of a subgroup of 22) WBS subjects showed a large number of hypometric and/or hypermetric saccades, and, also a left-right asymmetry in saccadic gains was observed in WBS. We conclude that the observed impairments in saccadic control are likely to affect the proper processing of visuo-spatial information.Numerous studies have described the poor visuo-spatial processing capacities of subjects with Williams-Beuren syndrome (WBS), a genetically based developmental disorder. Since visual perception and eye movements are closely related we hypothesized that the poor visuo-spatial processing capacities of subjects with WBS might be related to a poor saccadic control. Thereto, we recorded horizontal and vertical saccadic eye movements to targets using infrared video-oculography in 27 subjects with WBS and eight healthy controls. In the WBS group saccadic gains were highly variable, both between and within individual subjects, and they often needed more than one correction saccade to reach the target. Ten (out of a subgroup of 22) WBS subjects showed a large number of hypometric and/or hypermetric saccades, and, also a left-right asymmetry in saccadic gains was observed in WBS. We conclude that the observed impairments in saccadic control are likely to affect the proper processing of visuo-spatial information.
Numerous studies have described the poor visuo-spatial processing capacities of subjects with Williams-Beuren syndrome (WBS), a genetically based developmental disorder. Since visual perception and eye movements are closely related we hypothesized that the poor visuo-spatial processing capacities of subjects with WBS might be related to a poor saccadic control. Thereto, we recorded horizontal and vertical saccadic eye movements to targets using infrared video-oculography in 27 subjects with WBS and eight healthy controls. In the WBS group saccadic gains were highly variable, both between and within individual subjects, and they often needed more than one correction saccade to reach the target. Ten (out of a subgroup of 22) WBS subjects showed a large number of hypometric and/or hypermetric saccades, and, also a left-right asymmetry in saccadic gains was observed in WBS. We conclude that the observed impairments in saccadic control are likely to affect the proper processing of visuo-spatial information.
Author Govaerts, L.C.P.
Frens, M.A.
van Hagen, J.M.
de Coo, I.F.M.
van der Geest, J.N.
Lagers-van Haselen, G.C.
de Zeeuw, C.I.
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Issue 5
Keywords Genetic disorder
Cerebellum
Oculomotor
Accuracy
Eye movements
Spatial vision
Human
Cognition
Space perception
Saccadic eye movement
Williams syndrome
Vision
Complex syndrome
Language English
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Snippet Numerous studies have described the poor visuo-spatial processing capacities of subjects with Williams–Beuren syndrome (WBS), a genetically based developmental...
Numerous studies have described the poor visuo-spatial processing capacities of subjects with Williams-Beuren syndrome (WBS), a genetically based developmental...
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StartPage 569
SubjectTerms Accuracy
Adolescent
Adult
Adult and adolescent clinical studies
Biological and medical sciences
Cerebellar Ataxia - etiology
Cerebellum
Child
Eye movements
Female
Fixation, Ocular - physiology
Genetic disorder
Humans
Male
Medical sciences
Oculomotor
Organic mental disorders. Neuropsychology
Psychology. Psychoanalysis. Psychiatry
Psychomotor Performance
Psychopathology. Psychiatry
Reaction Time - physiology
Saccades - physiology
Spatial vision
Visual Perception - physiology
Williams Syndrome - complications
Title Saccade dysmetria in Williams–Beuren syndrome
URI https://dx.doi.org/10.1016/j.neuropsychologia.2003.11.003
https://www.ncbi.nlm.nih.gov/pubmed/14725795
https://www.proquest.com/docview/80101915
Volume 42
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