Handedness and corpus callosal morphology in Williams syndrome

Martens, Marilee A, Wilson, Sarah J, Chen, Jian, Wood, Amanda G and Reutens, David C 2013, Handedness and corpus callosal morphology in Williams syndrome, Development and psychopathology, vol. 25, no. 1, Special issue: gene–environment correlation in developmental psychopathology, pp. 253-260, doi: 10.1017/S0954579412001009.

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Title Handedness and corpus callosal morphology in Williams syndrome
Author(s) Martens, Marilee A
Wilson, Sarah J
Chen, Jian
Wood, Amanda GORCID iD for Wood, Amanda G orcid.org/0000-0002-1537-6858
Reutens, David C
Journal name Development and psychopathology
Volume number 25
Issue number 1
Season Special issue: gene–environment correlation in developmental psychopathology
Start page 253
End page 260
Total pages 8
Publisher Cambridge University Press
Place of publication Cambridge, Eng.
Publication date 2013-02
ISSN 0954-5794
1469-2198
Keyword(s) corpus callosal
Williams syndrome
neurodevelopmental genetic disorder
hemizygous deletion
Social Sciences
Psychology, Developmental
Psychology
Summary Williams syndrome is a neurodevelopmental genetic disorder caused by a hemizygous deletion on chromosome 7q11.23, resulting in atypical brain structure and function, including abnormal morphology of the corpus callosum. An influence of handedness on the size of the corpus callosum has been observed in studies of typical individuals, but handedness has not been taken into account in studies of callosal morphology in Williams syndrome. We hypothesized that callosal area is smaller and the size of the splenium and isthmus is reduced in individuals with Williams syndrome compared to healthy controls, and examined age, sex, and handedness effects on corpus callosal area. Structural magnetic resonance imaging scans were obtained on 25 individuals with Williams syndrome (18 right-handed, 7 left-handed) and 25 matched controls. We found that callosal thickness was significantly reduced in the splenium of Williams syndrome individuals compared to controls. We also found novel evidence that the callosal area was smaller in left-handed participants with Williams syndrome than their right-handed counterparts, with opposite findings observed in the control group. This novel finding may be associated with LIM-kinase hemizygosity, a characteristic of Williams syndrome. The findings may have significant clinical implications in future explorations of the Williams syndrome cognitive phenotype.
Language eng
DOI 10.1017/S0954579412001009
Indigenous content off
Field of Research 1701 Psychology
1702 Cognitive Sciences
HERDC Research category C1 Refereed article in a scholarly journal
Copyright notice ©2013, Cambridge University Press
Persistent URL http://hdl.handle.net/10536/DRO/DU:30128638

Document type: Journal Article
Collections: Faculty of Health
School of Psychology
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