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Fisher, M. H. – Journal of Intellectual Disability Research, 2014
Background: Individuals with Williams syndrome (WS) are reported to display increased sociability towards strangers, leading to increased social vulnerability. No research has examined real life interactions of adults with WS towards strangers and no interventions have been implemented to teach stranger safety skills to this population. Method:…
Descriptors: Genetic Disorders, Disabilities, Social Behavior, At Risk Persons
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Reilly, C. – Journal of Intellectual Disability Research, 2012
Background: A number of genetic conditions with associated intellectual disability and/or special educational needs have increasingly well-defined behavioural phenotypes. Thus, the concept of "behavioural phenotype" and aetiology of intellectual disability may be important with regard to school-based interventions. Method: The evidence for…
Descriptors: Guidelines, Teaching Methods, Genetics, Down Syndrome
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Riby, D. M.; Kirk, H.; Hanley, M.; Riby, L. M. – Journal of Intellectual Disability Research, 2014
Background: The developmental disorder Williams syndrome (WS) is characterised by a distinctive cognitive profile and an intriguing social phenotype. Individuals with the disorder are often highly social engaging with familiar and unfamiliar people and once in an interaction they often show subtle abnormalities of social behaviour. Atypically…
Descriptors: Genetic Disorders, Mental Retardation, Developmental Disabilities, Social Behavior
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Peebles, K. A.; Price, T. J. – Journal of Intellectual Disability Research, 2012
Background: In most individuals, injury results in activation of peripheral nociceptors (pain-sensing neurons of the peripheral nervous system) and amplification of central nervous system (CNS) pain pathways that serve as a disincentive to continue harmful behaviour; however, this may not be the case in some developmental disorders that cause…
Descriptors: Pain, Mental Retardation, Self Destructive Behavior, Neurology