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Behavioural indexes of callosal functioning in Williams syndrome
Andreia Santos1, Cécilie Rondan, Josette Mancini
1Mediterranean Institute of Cognitive Neurosciences, CNRS, Marseille, France. a.santos@incm.cnrs-mrs.fr
Journal of Neuropsychology
|April 1, 2009
Summary
Individuals with Williams syndrome (WS) show intact interhemispheric communication and hemispheric asymmetry. Despite structural brain differences, their visual processing and naming abilities are comparable to controls, though development differs.
Area of Science:
- Neurogenetics
- Cognitive Neuroscience
- Developmental Psychology
Background:
- Williams syndrome (WS) is a genetic disorder caused by a microdeletion on chromosome 7.
- Previous research indicates corpus callosum abnormalities in WS, but functional implications are unknown.
- Understanding interhemispheric communication is crucial for WS research.
Purpose of the Study:
- To investigate interhemispheric communication and hemispheric asymmetry in individuals with WS.
- To compare functional outcomes in WS against mental age-matched controls.
- To assess the impact of structural differences on callosal functionality.
Main Methods:
- Utilized a picture-naming task with bilateral and unilateral visual stimuli.
- Compared performance between individuals with WS and mental age-matched controls.
- Analyzed visual field advantages and hemispheric asymmetry.
Main Results:
- Both groups demonstrated a bilateral field advantage.
- Both groups showed a left visual field advantage on unilateral presentations.
- Controls exhibited age-related performance increases, unlike individuals with WS.
Conclusions:
- Interhemispheric communication and hemispheric asymmetry appear functionally intact in WS.
- Despite atypical development, core communication pathways are preserved.
- Findings suggest preserved visual processing and naming despite known structural variations.

