Literature DB >> 20181458

Prospective control abilities during visuo-manual tracking in children with 22q11.2 Deletion syndrome compared to age- and IQ-matched controls.

Katrijn Van Aken1, Ann Swillen, Marc Beirinckx, Luc Janssens, Karen Caeyenberghs, Bouwien Smits-Engelsman.   

Abstract

To examine whether children with a 22q11.2 Deletion syndrome (22q11.2DS) are able to use prospective control, 21 children with 22q11.2DS (mean age=9.6+/-1.9; mean FSIQ=73.05+/-10.2) and 21 control children (mean age=9.6+/-1.9; mean FSIQ=73.38+/-12.0) were asked to perform a visuo-manual tracking task in which they had to track a cursor rhythmically between 2 target zones. Children with 22q11.2DS performed worse than the age- and IQ-matched controls (higher absolute time and distance errors) suggesting that the 22q11.2DS group experiences an additional (syndrome specific) processing deficit that cannot be attributed to their lower intellectual abilities. The 22q11.2DS group neither the control group improved their tracking performance throughout five identical full feedback conditions of the tracking task possibly due to a slow visuo-motor adaptation process, a short span of attention and cognitive flexibility impairments. The results showed that both the 22q11.2DS group and the controls had difficulties anticipating the movement of the target (prospective control) and thus are assumed to rely more on feedback instead of on an internal representation of the movement. 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20181458     DOI: 10.1016/j.ridd.2010.01.002

Source DB:  PubMed          Journal:  Res Dev Disabil        ISSN: 0891-4222


  5 in total

Review 1.  22q11 deletion syndrome: a review of the neuropsychiatric features and their neurobiological basis.

Authors:  Chiara Squarcione; Maria Chiara Torti; Fabio Di Fabio; Massimo Biondi
Journal:  Neuropsychiatr Dis Treat       Date:  2013-12-04       Impact factor: 2.570

2.  Developmental coordination disorder, psychopathology and IQ in 22q11.2 deletion syndrome.

Authors:  Adam C Cunningham; Sue Delport; Wendy Cumines; Monica Busse; David E J Linden; Jeremy Hall; Michael J Owen; Marianne B M van den Bree
Journal:  Br J Psychiatry       Date:  2018-01       Impact factor: 10.671

3.  Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome.

Authors:  Adam C Cunningham; Liam Hill; Mark Mon-Williams; Kathryn J Peall; David E J Linden; Jeremy Hall; Michael J Owen; Marianne B M van den Bree
Journal:  J Neurodev Disord       Date:  2019-06-10       Impact factor: 4.074

4.  Assessing auditory processing endophenotypes associated with Schizophrenia in individuals with 22q11.2 deletion syndrome.

Authors:  Ana A Francisco; John J Foxe; Douwe J Horsthuis; Danielle DeMaio; Sophie Molholm
Journal:  Transl Psychiatry       Date:  2020-03-05       Impact factor: 6.222

5.  Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome.

Authors:  Liang Zhan; Lisanne M Jenkins; Aifeng Zhang; Giorgio Conte; Angus Forbes; Danielle Harvey; Kathleen Angkustsiri; Naomi J Goodrich-Hunsaker; Courtney Durdle; Aaron Lee; Cyndi Schumann; Owen Carmichael; Kristopher Kalish; Alex D Leow; Tony J Simon
Journal:  Hum Brain Mapp       Date:  2017-10-08       Impact factor: 5.038

  5 in total

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