Literature DB >> 17499412

Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome.

Joel P Bish1, Renee Chiodo, Victoria Mattei, Tony J Simon.   

Abstract

One of the defining cognitive characteristics of the chromosome 22q deletion syndrome (DS22q11.2) is visuospatial processing impairments. The purpose of this study was to investigate and extend the specific attentional profile of children with this disorder using both an object-based attention task and an inhibition of return task. A group of children with the disorder was compared in these tasks with a group of age-matched typically developing children. The children with DS22q11.2 demonstrated impaired spatially based orienting which is consistent with previous findings in this group. Strikingly, the children with DS22q11.2 also demonstrated an improved ability to use object-based cues, relative to the typically developing group. Finally, the children with DS22q11.2 demonstrated an intact inhibition of return system, however, it appears to be delayed developmentally.

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Year:  2007        PMID: 17499412      PMCID: PMC2727671          DOI: 10.1016/j.bandc.2007.03.007

Source DB:  PubMed          Journal:  Brain Cogn        ISSN: 0278-2626            Impact factor:   2.310


  29 in total

1.  Increased basal ganglia volumes in velo-cardio-facial syndrome (deletion 22q11.2).

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2.  A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

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Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

3.  Temporal perception in velo-cardio-facial syndrome.

Authors:  Martin Debbané; Bronwyn Glaser; Marianne Gex-Fabry; Stephan Eliez
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4.  Selective attention and the organization of visual information.

Authors:  J Duncan
Journal:  J Exp Psychol Gen       Date:  1984-12

5.  Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis.

Authors:  W R Kates; C P Burnette; E W Jabs; J Rutberg; A M Murphy; M Grados; M Geraghty; W E Kaufmann; G D Pearlson
Journal:  Biol Psychiatry       Date:  2001-04-15       Impact factor: 13.382

6.  Velocardiofacial syndrome: are structural changes in the temporal and mesial temporal regions related to schizophrenia?

Authors:  S Eliez; C M Blasey; E J Schmitt; C D White; D Hu; A L Reiss
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Review 7.  The 22q11.2 deletion syndrome.

Authors:  B S Emanuel; D McDonald-McGinn; S C Saitta; E H Zackai
Journal:  Adv Pediatr       Date:  2001

8.  Thalamic reductions in children with chromosome 22q11.2 deletion syndrome.

Authors:  Joel P Bish; Vy Nguyen; Lijun Ding; Samantha Ferrante; Tony J Simon
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9.  Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

Authors:  J Burn; A Takao; D Wilson; I Cross; K Momma; R Wadey; P Scambler; J Goodship
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

10.  A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.

Authors:  R J Shprintzen; R B Goldberg; M L Lewin; E J Sidoti; M D Berkman; R V Argamaso; D Young
Journal:  Cleft Palate J       Date:  1978-01
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  17 in total

Review 1.  The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.

Authors:  Liam J Drew; Gregg W Crabtree; Sander Markx; Kimberly L Stark; Florence Chaverneff; Bin Xu; Jun Mukai; Karine Fenelon; Pei-Ken Hsu; Joseph A Gogos; Maria Karayiorgou
Journal:  Int J Dev Neurosci       Date:  2010-10-08       Impact factor: 2.457

Review 2.  A new account of the neurocognitive foundations of impairments in space, time and number processing in children with chromosome 22q11.2 deletion syndrome.

Authors:  Tony J Simon
Journal:  Dev Disabil Res Rev       Date:  2008

Review 3.  Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

Authors:  Daniel Paul Eisenberg; Mbemba Jabbi; Karen Faith Berman
Journal:  Neuroimage       Date:  2010-03-03       Impact factor: 6.556

Review 4.  22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.

Authors:  Maria Karayiorgou; Tony J Simon; Joseph A Gogos
Journal:  Nat Rev Neurosci       Date:  2010-06       Impact factor: 34.870

5.  Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndrome.

Authors:  Yi Deng; Naomi J Goodrich-Hunsaker; Margarita Cabaral; David G Amaral; Michael H Buonocore; Danielle Harvey; Kristopher Kalish; Owen T Carmichael; Cynthia M Schumann; Aaron Lee; Robert F Dougherty; Lee M Perry; Brian A Wandell; Tony J Simon
Journal:  Psychiatry Res       Date:  2015-02-11       Impact factor: 3.222

6.  Attentional functioning in individuals with 22q11 deletion syndrome: insight from ERPs.

Authors:  Daniela Mannarelli; Caterina Pauletti; Tommaso Accinni; Luca Carlone; Marianna Frascarelli; Guido Maria Lattanzi; Antonio Currà; Francesco Fattapposta
Journal:  J Neural Transm (Vienna)       Date:  2018-03-08       Impact factor: 3.575

Review 7.  Clues to the foundations of numerical cognitive impairments: evidence from genetic disorders.

Authors:  Tony J Simon
Journal:  Dev Neuropsychol       Date:  2011       Impact factor: 2.253

8.  Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory.

Authors:  Ling M Wong; Tracy Riggins; Danielle Harvey; Margarita Cabaral; Tony J Simon
Journal:  Am J Intellect Dev Disabil       Date:  2014-03

9.  The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety.

Authors:  Julia A Scott; Naomi Goodrich-Hunsaker; Kristopher Kalish; Aaron Lee; Michael R Hunsaker; Cynthia M Schumann; Owen T Carmichael; Tony J Simon
Journal:  J Psychiatry Neurosci       Date:  2016-04       Impact factor: 6.186

10.  A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndrome.

Authors:  Heather M Shapiro; Yukari Takarae; Danielle J Harvey; Margarita H Cabaral; Tony J Simon
Journal:  J Neurodev Disord       Date:  2012-02-15       Impact factor: 4.025

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