Williams syndrome is a rare genetic condition (estimated to occur in 1/7,500 births) that causes medical and developmental problems. Williams syndrome is associated with an unusual pattern of strengths and weaknesses in linguistic and cognitive profiles, as well as intellectual disability. It is present at birth and affects males and females equally. It can occur in all ethnic groups and has been identified in countries throughout the world.
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Elisabeth Dykens, Ph.D.
Professor of Psychology, Psychiatry & Behavioral Sciences, and Pediatrics; Co-Director, Vanderbilt Kennedy Center for Excellence in Developmental Disabilities
Elizabeth Roof, M.A.
Senior Research Specialist, Prader-Willi Syndrome and Williams Syndrome Research Projects
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