Literature DB >> 11104544

The Williams syndrome cognitive profile.

C B Mervis1, B F Robinson, J Bertrand, C A Morris, B P Klein-Tasman, S C Armstrong.   

Abstract

Williams syndrome is a rare neurodevelopmental disorder caused by a hemizygous deletion of approximately 1.5 megabases on chromosome 7q11.23. In this article, we outline a Williams Syndrome Cognitive Profile (WSCP) that operationalizes the cognitive characteristics of the syndrome using measures of absolute and relative performance on subtests of the Differential Abilities Scales (Elliot, 1990a). Testing confirmed excellent sensitivity and specificity scores for the WSCP. Seventy-four of 84 individuals with Williams syndrome fit the WSCP while only 4 participants in a contrast group met all of the WSCP criteria. It was also found that the WSCP does not vary greatly with chronological age or overall level of cognitive ability for individuals with Williams syndrome. Possible applications for the WSCP include psychoeducational evaluation and empirical research such as the search for genotype/phenotype relations in this genetically based syndrome. Copyright 2000 Academic Press.

Entities:  

Mesh:

Year:  2000        PMID: 11104544     DOI: 10.1006/brcg.2000.1232

Source DB:  PubMed          Journal:  Brain Cogn        ISSN: 0278-2626            Impact factor:   2.310


  105 in total

1.  Neuropsychological components of intellectual disability: the contributions of immediate, working, and associative memory.

Authors:  Jamie O Edgin; Bruce F Pennington; Carolyn B Mervis
Journal:  J Intellect Disabil Res       Date:  2010-05

2.  Small Subitizing Range in People with Williams syndrome.

Authors:  Kirsten O'Hearn; James E Hoffman; Barbara Landau
Journal:  Vis cogn       Date:  2011-03

Review 3.  Methodological issues in group-matching designs: alpha levels for control variable comparisons and measurement characteristics of control and target variables.

Authors:  Carolyn B Mervis; Bonita P Klein-Tasman
Journal:  J Autism Dev Disord       Date:  2004-02

Review 4.  Cognitive and behavioral characteristics of children with Williams syndrome: implications for intervention approaches.

Authors:  Carolyn B Mervis; Angela E John
Journal:  Am J Med Genet C Semin Med Genet       Date:  2010-05-15       Impact factor: 3.908

5.  Honing in on the social phenotype in Williams syndrome using multiple measures and multiple raters.

Authors:  Bonita P Klein-Tasman; Kirsten T Li-Barber; Erin T Magargee
Journal:  J Autism Dev Disord       Date:  2011-03

6.  Orientation perception in Williams Syndrome: discrimination and integration.

Authors:  Melanie Palomares; Barbara Landau; Howard Egeth
Journal:  Brain Cogn       Date:  2009-02-23       Impact factor: 2.310

7.  Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content.

Authors:  Karen E Muñoz; Andreas Meyer-Lindenberg; Ahmad R Hariri; Carolyn B Mervis; Venkata S Mattay; Colleen A Morris; Karen Faith Berman
Journal:  Neuroimage       Date:  2009-12-11       Impact factor: 6.556

8.  Sudden unexpected death in a toddler with Williams syndrome.

Authors:  Henry F Krous; Carter Wahl; Amy E Chadwick
Journal:  Forensic Sci Med Pathol       Date:  2008-04-04       Impact factor: 2.007

9.  Viewing social scenes: a visual scan-path study comparing fragile X syndrome and Williams syndrome.

Authors:  Tracey A Williams; Melanie A Porter; Robyn Langdon
Journal:  J Autism Dev Disord       Date:  2013-08

Review 10.  Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome.

Authors:  Barbara R Pober; Mark Johnson; Zsolt Urban
Journal:  J Clin Invest       Date:  2008-05       Impact factor: 14.808

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