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Elsabbagh, M.; Cohen, H.; Cohen, M.; Rosen, S.; Karmiloff-Smith, A. – Journal of Intellectual Disability Research, 2011
Background: Williams Syndrome (WS) is a neurodevelopmental disorder of genetic origin, characterised by relative proficiency in language in the face of serious impairment in several other domains. Individuals with WS display an unusual sensitivity to noise, known as hyperacusis. Methods: In this study, we examined the extent to which hyperacusis…
Descriptors: Genetic Disorders, Mental Retardation, Congenital Impairments, Individual Differences
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Key, A. P. F.; Dykens, E. M. – Journal of Intellectual Disability Research, 2008
Background: Prader-Willi syndrome (PWS) is a genetic disorder associated with intellectual disabilities, compulsivity, hyperphagia and increased risks of life-threatening obesity. Food preferences in people with PWS are well documented, but research has yet to focus on other properties of food in PWS, including composition and suitability for…
Descriptors: Individual Differences, Obesity, Mental Retardation, Genetics