Literature DB >> 15753050

Cognitive heterogeneity in Williams syndrome.

Melanie A Porter1, Max Coltheart.   

Abstract

This study used the Woodcock-Johnson Tests of Cognitive Ability-Revised to investigate a wide range of cognitive abilities in people with Williams syndrome (WS). It involved a comparatively large sample of 31 people with WS, but took a case-series approach. The study addressed the widespread claims of a characteristic "WS cognitive profile" by looking for heterogeneity rather than homogeneity. People with WS showed a variety of preserved (significantly above mental age [MA]), expected (at MA), and significantly impaired (significantly below MA) levels of functioning. Such results provide clear evidence for heterogeneity in cognitive functions within WS. We found the most homogeneity on a test of phonological processing and a test of phonological short-term memory, with half of the WS sample performing at MA levels on these tests. Interestingly, no WS individual showed a weakness on a test of nonverbal reasoning, and only one WS individual showed a weakness on a test of verbal comprehension. In addition, we found that strengths on analysis-synthesis and verbal analogies occurred only for WS individuals with an MA less than 5.5 years (our sample median MA); people with an MA greater than 5.5 years performed at MA level on these 2 tests. Results also provided preliminary evidence for distinct subgroups of WS people based on their cognitive strengths and weaknesses on a broad range of cognitive functions. On the basis of the findings, caution should be made in declaring a single cognitive profile that is characteristic of all individuals with WS. Just as there is heterogeneity in genetic and physical anomalies within WS, not all WS individuals share the same cognitive strengths and weaknesses. Also, not all WS individuals show the profile of a strength in verbal abilities and a weakness in spatial functions.

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Year:  2005        PMID: 15753050     DOI: 10.1207/s15326942dn2702_5

Source DB:  PubMed          Journal:  Dev Neuropsychol        ISSN: 1532-6942            Impact factor:   2.253


  19 in total

1.  An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism.

Authors:  Lisa Edelmann; Aaron Prosnitz; Sherly Pardo; Jahnavi Bhatt; Ninette Cohen; Tara Lauriat; Leonid Ouchanov; Patricia J González; Elina R Manghi; Pamela Bondy; Marcela Esquivel; Silvia Monge; Marietha F Delgado; Alessandra Splendore; Uta Francke; Barbara K Burton; L Alison McInnes
Journal:  J Med Genet       Date:  2006-09-13       Impact factor: 6.318

2.  Relations between social-perceptual ability in multi- and unisensory contexts, autonomic reactivity, and social functioning in individuals with Williams syndrome.

Authors:  Anna Järvinen; Rowena Ng; Davide Crivelli; Andrew J Arnold; Nicholas Woo-VonHoogenstyn; Ursula Bellugi
Journal:  Neuropsychologia       Date:  2015-05-19       Impact factor: 3.139

3.  Patterns of Sensitivity to Emotion in Children with Williams Syndrome and Autism: Relations Between Autonomic Nervous System Reactivity and Social Functioning.

Authors:  Anna Järvinen; Rowena Ng; Davide Crivelli; Dirk Neumann; Mark Grichanik; Andrew J Arnold; Philip Lai; Doris Trauner; Ursula Bellugi
Journal:  J Autism Dev Disord       Date:  2015-08

4.  Theory of mind in Williams syndrome assessed using a nonverbal task.

Authors:  Melanie A Porter; Max Coltheart; Robyn Langdon
Journal:  J Autism Dev Disord       Date:  2008-05

5.  The interplay between anxiety and social functioning in Williams syndrome.

Authors:  Deborah M Riby; Mary Hanley; Hannah Kirk; Fiona Clark; Katie Little; Ruth Fleck; Emily Janes; Linzi Kelso; Fionnuala O'Kane; Rachel Cole-Fletcher; Marianne Hvistendahl Allday; Darren Hocking; Kim Cornish; Jacqui Rodgers
Journal:  J Autism Dev Disord       Date:  2014-05

6.  Comparing the broad socio-cognitive profile of youth with Williams syndrome and 22q11.2 deletion syndrome.

Authors:  O Weisman; R Feldman; M Burg-Malki; M Keren; R Geva; G Diesendruck; D Gothelf
Journal:  J Intellect Disabil Res       Date:  2017-10-08

7.  Autonomic response to approachability characteristics, approach behavior, and social functioning in Williams syndrome.

Authors:  Anna Järvinen; Rowena Ng; Ursula Bellugi
Journal:  Neuropsychologia       Date:  2015-10-13       Impact factor: 3.139

8.  A direct comparison of local-global integration in autism and other developmental disorders: implications for the central coherence hypothesis.

Authors:  Inês Bernardino; Susana Mouga; Joana Almeida; Marieke van Asselen; Guiomar Oliveira; Miguel Castelo-Branco
Journal:  PLoS One       Date:  2012-06-19       Impact factor: 3.240

9.  Sensory Processing in Williams Syndrome: Individual differences and changes over time.

Authors:  Bradley Powell; Jo Van Herwegen
Journal:  J Autism Dev Disord       Date:  2021-07-21

10.  A role for transcription factor GTF2IRD2 in executive function in Williams-Beuren syndrome.

Authors:  Melanie A Porter; Carol Dobson-Stone; John B J Kwok; Peter R Schofield; William Beckett; May Tassabehji
Journal:  PLoS One       Date:  2012-10-31       Impact factor: 3.240

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