Literature DB >> 19118537

Brain structural differences associated with the behavioural phenotype in children with Williams syndrome.

Linda E Campbell1, Eileen Daly, Fiona Toal, Angela Stevens, Rayna Azuma, Annette Karmiloff-Smith, Declan G M Murphy, Kieran C Murphy.   

Abstract

BACKGROUND: We investigated structural brain morphology of intellectually disabled children with Williams (WS) syndrome and its relationship to the behavioural phenotype.
METHODS: We compared the neuroanatomy of 15 children (mean age:13+/-2) with WS and 15 age/gender-matched healthy children using a manual region-of-interest analysis to measure bulk (white+grey) tissue volumes and unbiased fully-automated voxel-based morphometry to assess differences in grey/white matter throughout the brain. Ratings of abnormal behaviours were correlated with brain structure.
RESULTS: Compared to controls, the brains of children with WS had a decreased volume of the right parieto-occipital regions and basal ganglia. We identified reductions of grey matter of the parieto-occipital regions, left putamen/globus pallidus and thalamus; and in white matter of the basal ganglia and right posterior cingulate gyrus. In contrast, significant increases of grey matter were identified in the frontal lobes, anterior cingulate gyrus, left temporal lobe, and of white matter bilaterally in the anterior cingulate. Inattention in WS was correlated with volumetric differences in the frontal lobes, caudate nucleus and cerebellum, and hyperactivity was related to differences in the left temporal and parietal lobes and cerebellum. Finally, ratings of peer problems were related to differences in the temporal lobes, right basal ganglia and frontal lobe.
CONCLUSIONS: In one of the first studies of brain structure in intellectually disabled children with WS using voxel-based morphometry, our findings suggest that this group has specific differences in grey/white matter morphology. In addition, it was found that structural differences were correlated to ratings of inattention, hyperactivity and peer problems in children with WS.

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Year:  2008        PMID: 19118537     DOI: 10.1016/j.brainres.2008.11.101

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  24 in total

1.  Preliminary evidence of abnormal white matter related to the fusiform gyrus in Williams syndrome: a diffusion tensor imaging tractography study.

Authors:  B W Haas; F Hoeft; N Barnea-Goraly; G Golarai; U Bellugi; A L Reiss
Journal:  Genes Brain Behav       Date:  2011-10-19       Impact factor: 3.449

2.  White matter integrity deficits in prefrontal-amygdala pathways in Williams syndrome.

Authors:  Suzanne N Avery; Tricia A Thornton-Wells; Adam W Anderson; Jennifer Urbano Blackford
Journal:  Neuroimage       Date:  2011-10-08       Impact factor: 6.556

Review 3.  Conceptualizing neurodevelopmental disorders through a mechanistic understanding of fragile X syndrome and Williams syndrome.

Authors:  Lawrence K Fung; Eve-Marie Quintin; Brian W Haas; Allan L Reiss
Journal:  Curr Opin Neurol       Date:  2012-04       Impact factor: 5.710

4.  The 7q11.23 Protein DNAJC30 Interacts with ATP Synthase and Links Mitochondria to Brain Development.

Authors:  Andrew T N Tebbenkamp; Luis Varela; Jinmyung Choi; Miguel I Paredes; Alice M Giani; Jae Eun Song; Matija Sestan-Pesa; Daniel Franjic; André M M Sousa; Zhong-Wu Liu; Mingfeng Li; Candace Bichsel; Marco Koch; Klara Szigeti-Buck; Fuchen Liu; Zhuo Li; Yuka I Kawasawa; Constantinos D Paspalas; Yann S Mineur; Paolo Prontera; Giuseppe Merla; Marina R Picciotto; Amy F T Arnsten; Tamas L Horvath; Nenad Sestan
Journal:  Cell       Date:  2018-11-01       Impact factor: 41.582

5.  Williams syndrome hemideletion and LIMK1 variation both affect dorsal stream functional connectivity.

Authors:  Michael D Gregory; Carolyn B Mervis; Maxwell L Elliott; J Shane Kippenhan; Tiffany Nash; Jasmin B Czarapata; Ranjani Prabhakaran; Katherine Roe; Daniel P Eisenberg; Philip D Kohn; Karen F Berman
Journal:  Brain       Date:  2019-12-01       Impact factor: 13.501

Review 6.  Abnormal structure or function of the amygdala is a common component of neurodevelopmental disorders.

Authors:  Cynthia M Schumann; Melissa D Bauman; David G Amaral
Journal:  Neuropsychologia       Date:  2010-10-13       Impact factor: 3.139

Review 7.  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

8.  Leftward lateralization of auditory cortex underlies holistic sound perception in Williams syndrome.

Authors:  Martina Wengenroth; Maria Blatow; Martin Bendszus; Peter Schneider
Journal:  PLoS One       Date:  2010-08-23       Impact factor: 3.240

9.  Altered microstructure within social-cognitive brain networks during childhood in Williams syndrome.

Authors:  Brian W Haas; Naama Barnea-Goraly; Kristen E Sheau; Bun Yamagata; Shruti Ullas; Allan L Reiss
Journal:  Cereb Cortex       Date:  2013-05-24       Impact factor: 5.357

10.  Neurophysiological Correlates of Dynamic Beat Tracking in Individuals With Williams Syndrome.

Authors:  Anna Kasdan; Reyna L Gordon; Miriam D Lense
Journal:  Biol Psychiatry Cogn Neurosci Neuroimaging       Date:  2020-10-22
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