Literature DB >> 15714897

Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome.

Tony J Simon1, Carrie E Bearden, Donna McDonald Mc-Ginn, Elaine Zackai.   

Abstract

This article presents some of the earliest evidence of visuospatial and numerical cognitive deficits in children with the chromosome 22q11.2 deletion syndrome; a common but ill-understood genetic disorder resulting in medical complications, cognitive impairment, and brain morphologic changes. Relative to a group of typically developing controls, deleted children performed more poorly on tests of visual attentional orienting, visual enumeration and relative numerical magnitude judgment. Results showed that performance deficits in children with the deletion could not be explained by a global deficit in psychomotor speed. Instead, our findings are supportive of the hypothesis that visuospatial and numerical deficits in children with the chromosome 22q11.2 deletion are due, at least in part, to posterior parietal dysfunction.

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Year:  2005        PMID: 15714897      PMCID: PMC4318636          DOI: 10.1016/s0010-9452(08)70889-x

Source DB:  PubMed          Journal:  Cortex        ISSN: 0010-9452            Impact factor:   4.027


  42 in total

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

2.  Voluntary orienting is dissociated from target detection in human posterior parietal cortex.

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Journal:  Nat Neurosci       Date:  2000-03       Impact factor: 24.884

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

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Journal:  Biol Psychiatry       Date:  2001-04-15       Impact factor: 13.382

4.  Superior parietal cortex activation during spatial attention shifts and visual feature conjunction.

Authors:  M Corbetta; G L Shulman; F M Miezin; S E Petersen
Journal:  Science       Date:  1995-11-03       Impact factor: 47.728

5.  Cognitive profiles associated with the fra(X) syndrome in males and females.

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Journal:  Am J Med Genet       Date:  1991-03-15

6.  Metabolic abnormalities detected by 1H-MRS in dyscalculia and dysgraphia.

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Journal:  Neurology       Date:  1999-08-11       Impact factor: 9.910

7.  Development itself is the key to understanding developmental disorders.

Authors:  A Karmiloff-Smith
Journal:  Trends Cogn Sci       Date:  1998-10-01       Impact factor: 20.229

8.  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

Review 9.  Varieties of numerical abilities.

Authors:  S Dehaene
Journal:  Cognition       Date:  1992-08

10.  Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.

Authors:  D A Driscoll; N B Spinner; M L Budarf; D M McDonald-McGinn; E H Zackai; R B Goldberg; R J Shprintzen; H M Saal; J Zonana; M C Jones
Journal:  Am J Med Genet       Date:  1992-09-15
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  51 in total

1.  Small Subitizing Range in People with Williams syndrome.

Authors:  Kirsten O'Hearn; James E Hoffman; Barbara Landau
Journal:  Vis cogn       Date:  2011-03

2.  Atypical functional brain activation during a multiple object tracking task in girls with Turner syndrome: neurocorrelates of reduced spatiotemporal resolution.

Authors:  Elliott A Beaton; Joel Stoddard; Song Lai; John Lackey; Jianrong Shi; Judith L Ross; Tony J Simon
Journal:  Am J Intellect Dev Disabil       Date:  2010-03

3.  Working Memory Impairments in Chromosome 22q11.2 Deletion Syndrome: The Roles of Anxiety and Stress Physiology.

Authors:  Ashley F P Sanders; Diana A Hobbs; David D Stephenson; Robert D Laird; Elliott A Beaton
Journal:  J Autism Dev Disord       Date:  2017-04

4.  Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome.

Authors:  Alexei M C Machado; Tony J Simon; Vy Nguyen; Donna M McDonald-McGinn; Elaine H Zackai; James C Gee
Journal:  Brain Res       Date:  2006-12-13       Impact factor: 3.252

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

Authors:  Joel P Bish; Renee Chiodo; Victoria Mattei; Tony J Simon
Journal:  Brain Cogn       Date:  2007-05-11       Impact factor: 2.310

Review 6.  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 7.  Neural phenotypes of common and rare genetic variants.

Authors:  Carrie E Bearden; David C Glahn; Agatha D Lee; Ming-Chang Chiang; Theo G M van Erp; Tyrone D Cannon; Allan L Reiss; Arthur W Toga; Paul M Thompson
Journal:  Biol Psychol       Date:  2008-02-23       Impact factor: 3.251

Review 8.  Cognitive characteristics of children with genetic syndromes.

Authors:  Tony J Simon
Journal:  Child Adolesc Psychiatr Clin N Am       Date:  2007-07

Review 9.  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 10.  Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome.

Authors:  Matthew J Schreiner; Maria T Lazaro; Maria Jalbrzikowski; Carrie E Bearden
Journal:  Neuropharmacology       Date:  2012-10-23       Impact factor: 5.250

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