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Direct linkPalomares, Melanie; Landau, Barbara; Egeth, Howard – Brain and Cognition, 2009
Williams Syndrome (WS) is a rare neurodevelopmental disorder, which stems from a genetic deletion on chromosome 7 and causes a profound weakness in visuospatial cognition. Our current study explores how orientation perception may contribute to the visuospatial deficits in WS. In Experiment 1, we found that WS individuals and normal 3-4 year olds…
Descriptors: Developmental Disabilities, Neurological Impairments, Spatial Ability, Young Children
