Literature DB >> 28745018

A comparison between linguistic skills and socio-communicative abilities in Williams syndrome.

P Alfieri1, D Menghini1, L Marotta2, L De Peppo3, L Ravà4, F Salvaguardia1, C Varuzza1, S Vicari1.   

Abstract

BACKGROUND: Individuals with Williams syndrome (WS) show a disharmonic linguistic profile with a clear pattern of strengths and weaknesses. Despite their sociable nature, atypical socio-communicative abilities and deficits in communication and relationship with others have been found. AIM: The aim of the present study was to investigate whether linguistic skills (LS) were in line with the pragmatic and social use of language and the cognitive development of 32 individuals with WS (18 boys and 14 girls) with a mean chronological age of 12.3 (±4.4) years. To examine the relationship between language and mental age (MA) at different ages, the issue was investigated in children and adolescents/young adults with WS.
METHOD: Measures of LS, including lexical and morphosyntactic competences, and adaptive socio-communicative abilities (ASCA), pertaining to the use of language in daily living social context, were compared with the MA of participants. In a second step, participants with WS were split into two subgroups based on age, and the relationship between LS, ASCA and MA was studied.
RESULTS: Although expressive and receptive LS were generally found to be in line with or better than would be expected for MA, specific deficits in receptive ASCA were documented. LS and ASCA appeared to have a different evolution during the different time windows considered.
CONCLUSIONS: Our results underlined the importance of assessing linguistic abilities in the context of adaptive functioning, to guide educational and rehabilitative strategies for individuals with WS.
© 2017 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and John Wiley & Sons Ltd.

Entities:  

Keywords:  adaptive behaviour; genetic syndrome; intellectual disability; language

Mesh:

Year:  2017        PMID: 28745018     DOI: 10.1111/jir.12401

Source DB:  PubMed          Journal:  J Intellect Disabil Res        ISSN: 0964-2633


  4 in total

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Journal:  Front Psychiatry       Date:  2022-05-06       Impact factor: 5.435

2.  7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling.

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Journal:  Brain Sci       Date:  2020-11-11

3.  Differences and Similarities in Adaptive Functioning between Children with Autism Spectrum Disorder and Williams-Beuren Syndrome: A Longitudinal Study.

Authors:  Paolo Alfieri; Francesco Scibelli; Federica Alice Maria Montanaro; Maria Cristina Digilio; Lucilla Ravà; Giovanni Valeri; Stefano Vicari
Journal:  Genes (Basel)       Date:  2022-07-16       Impact factor: 4.141

4.  Cooperative Parent-Mediated Therapy in Children with Fragile X Syndrome and Williams Beuren Syndrome: A Pilot RCT Study of a Transdiagnostic Intervention-Preliminary Data.

Authors:  Paolo Alfieri; Francesco Scibelli; Laura Casula; Simone Piga; Eleonora Napoli; Giovanni Valeri; Stefano Vicari
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  4 in total

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