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Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

BACKGROUND: Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000 live births with a complex and variable presentation that includes medical, socioemotional and psychological symptoms with intellectual impairment. Cognitive impairments in spatiotemporal and visuospatial at...

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Autores principales: Cabaral, Margarita H, Beaton, Elliott A, Stoddard, Joel, Simon, Tony J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374294/
https://www.ncbi.nlm.nih.gov/pubmed/22958454
http://dx.doi.org/10.1186/1866-1955-4-6
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author Cabaral, Margarita H
Beaton, Elliott A
Stoddard, Joel
Simon, Tony J
author_facet Cabaral, Margarita H
Beaton, Elliott A
Stoddard, Joel
Simon, Tony J
author_sort Cabaral, Margarita H
collection PubMed
description BACKGROUND: Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000 live births with a complex and variable presentation that includes medical, socioemotional and psychological symptoms with intellectual impairment. Cognitive impairments in spatiotemporal and visuospatial attention have also been reported. However, maintenance of selective attention to dynamic and interacting objects has not been systematically investigated in children with 22q11.2DS. METHODS: We used a multiple object tracking task to assay capacity and resolution performance of children with 22q11.2DS aged 7 to 14 years versus age-matched typically developing (TD) peers. RESULTS: Children with 22q11.2DS but not TD children demonstrated impaired performance when task demands increased due to an increase in the number of targets presented, but not from an increase in object speed. Task performance in children with 22q11.2DS was also unrelated to intelligence or measures of attention deficit hyperactivity disorder. CONCLUSIONS: These findings suggest that children with 22q11.2DS may be particularly susceptible to dynamic crowding of objects with increasing cognitive demands related to monitoring multiple targets reflecting a reduced acuity in spatiotemporal cognitive representation.
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spelling pubmed-33742942012-07-17 Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome Cabaral, Margarita H Beaton, Elliott A Stoddard, Joel Simon, Tony J J Neurodev Disord Research BACKGROUND: Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000 live births with a complex and variable presentation that includes medical, socioemotional and psychological symptoms with intellectual impairment. Cognitive impairments in spatiotemporal and visuospatial attention have also been reported. However, maintenance of selective attention to dynamic and interacting objects has not been systematically investigated in children with 22q11.2DS. METHODS: We used a multiple object tracking task to assay capacity and resolution performance of children with 22q11.2DS aged 7 to 14 years versus age-matched typically developing (TD) peers. RESULTS: Children with 22q11.2DS but not TD children demonstrated impaired performance when task demands increased due to an increase in the number of targets presented, but not from an increase in object speed. Task performance in children with 22q11.2DS was also unrelated to intelligence or measures of attention deficit hyperactivity disorder. CONCLUSIONS: These findings suggest that children with 22q11.2DS may be particularly susceptible to dynamic crowding of objects with increasing cognitive demands related to monitoring multiple targets reflecting a reduced acuity in spatiotemporal cognitive representation. Springer 2012 2012-04-12 /pmc/articles/PMC3374294/ /pubmed/22958454 http://dx.doi.org/10.1186/1866-1955-4-6 Text en Copyright ©2012 Cabaral et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Cabaral, Margarita H
Beaton, Elliott A
Stoddard, Joel
Simon, Tony J
Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
title Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
title_full Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
title_fullStr Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
title_full_unstemmed Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
title_short Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
title_sort impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374294/
https://www.ncbi.nlm.nih.gov/pubmed/22958454
http://dx.doi.org/10.1186/1866-1955-4-6
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