Literature DB >> 11339378

Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2).

S Eliez1, C M Blasey, V Menon, C D White, J E Schmitt, A L Reiss.   

Abstract

PURPOSE: Children with velocardiofacial syndrome (VCFS) often have deficits in mathematical reasoning. Previous research has suggested that structural abnormalities in the parietal lobe region might underlie these deficits. The present study utilized functional magnetic resonance imaging (fMRI) to explore the relationship between brain function and mathematical performance in VCFS.
METHODS: Eight children with VCFS and eight comparison subjects underwent fMRI scanning and completed an arithmetic computation task.
RESULTS: In the VCFS group, increased activation was observed in the left supramarginal gyrus (LSMG) as the task difficulty increased.
CONCLUSION: Aberrant LSMG activation, possibly due to structural deficits of the left parietal lobe, may explain decrements in arithmetic performance observed in VCFS.

Entities:  

Mesh:

Year:  2001        PMID: 11339378     DOI: 10.1097/00125817-200101000-00011

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  19 in total

Review 1.  Imaging of neurogenetic and neurometabolic disorders of childhood.

Authors:  Andrea Gropman
Journal:  Curr Neurol Neurosci Rep       Date:  2004-03       Impact factor: 5.081

Review 2.  Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome.

Authors:  E Walter; P K Mazaika; A L Reiss
Journal:  Neuroscience       Date:  2009-04-17       Impact factor: 3.590

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

4.  Time-Resolved and Spatio-Temporal Analysis of Complex Cognitive Processes and their Role in Disorders like Developmental Dyscalculia.

Authors:  István Akos Mórocz; Firdaus Janoos; Peter van Gelderen; David Manor; Avi Karni; Zvia Breznitz; Michael von Aster; Tammar Kushnir; Ruth Shalev
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Review 5.  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

Review 6.  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

7.  Velo-Cardio-Facial Syndrome.

Authors:  Doron Gothelf; Amos Frisch; Elena Michaelovsky; Abraham Weizman; Robert J Shprintzen
Journal:  J Ment Health Res Intellect Disabil       Date:  2009-04

8.  Overlapping numerical cognition impairments in children with chromosome 22q11.2 deletion or Turner syndromes.

Authors:  T J Simon; Y Takarae; T DeBoer; D M McDonald-McGinn; E H Zackai; J L Ross
Journal:  Neuropsychologia       Date:  2007-08-26       Impact factor: 3.139

9.  Potential Role of Cortisol in Social and Memory Impairments in Individuals with 22q11.2 Deletion Syndrome.

Authors:  Daniel Jacobson; Megan Bursch; Renee Lajiness-O'Neill
Journal:  J Pediatr Genet       Date:  2016-06-20

10.  White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging.

Authors:  Julio Villalon-Reina; Neda Jahanshad; Elliott Beaton; Arthur W Toga; Paul M Thompson; Tony J Simon
Journal:  Neuroimage       Date:  2013-04-18       Impact factor: 6.556

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