Literature DB >> 10899809

Williams syndrome: cognition, personality, and adaptive behavior.

C B Mervis1, B P Klein-Tasman.   

Abstract

Williams syndrome is caused by a microdeletion of at least 16 genes on chromosome 7q11.23. The syndrome results in mild to moderate mental retardation or learning disability. The behavioral phenotype for Williams syndrome is characterized by a distinctive cognitive profile and an unusual personality profile. Relative to overall level of intellectual ability, individuals with Williams syndrome typically show a clear strength in auditory rote memory, a strength in language, and an extreme weakness in visuospatial construction. The personality of individuals with Williams syndrome involves high sociability, overfriendliness, and empathy, with an undercurrent of anxiety related to social situations. The adaptive behavior profile for Williams syndrome involves clear strength in socialization skills (especially interpersonal skills related to initiating social interaction), strength in communication, and clear weakness in daily living skills and motor skills, relative to overall level of adaptive behavior functioning. Literature relevant to each of the components of the Williams syndrome behavioral phenotype is reviewed, including operationalizations of the Williams syndrome cognitive profile and the Williams syndrome personality profile. The sensitivity and specificity of these profiles for Williams syndrome, relative to individuals with other syndromes or mental retardation or borderline normal intelligence of unknown etiology, is considered. The adaptive behavior profile is discussed in relation to the cognitive and personality profiles. The importance of operationalizations of crucial components of the behavioral phenotype for the study of genotype/phenotype correlations in Williams syndrome is stressed. MRDD Research Reviews 2000;6:148-158. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10899809     DOI: 10.1002/1098-2779(2000)6:2<148::AID-MRDD10>3.0.CO;2-T

Source DB:  PubMed          Journal:  Ment Retard Dev Disabil Res Rev        ISSN: 1080-4013


  71 in total

1.  Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.

Authors:  Udaya DeSilva; Laura Elnitski; Jacquelyn R Idol; Johannah L Doyle; Weiniu Gan; James W Thomas; Scott Schwartz; Nicole L Dietrich; Stephen M Beckstrom-Sternberg; Jennifer C McDowell; Robert W Blakesley; Gerard G Bouffard; Pamela J Thomas; Jeffrey W Touchman; Webb Miller; Eric D Green
Journal:  Genome Res       Date:  2002-01       Impact factor: 9.043

Review 2.  Language phenotypes and intervention planning: bridging research and practice.

Authors:  Deborah J Fidler; Amy Philofsky; Susan L Hepburn
Journal:  Ment Retard Dev Disabil Res Rev       Date:  2007

3.  Callosal morphology in Williams syndrome: a new evaluation of shape and thickness.

Authors:  Eileen Luders; Margherita Di Paola; Francesco Tomaiuolo; Paul M Thompson; Arthur W Toga; Stefano Vicari; Michael Petrides; Carlo Caltagirone
Journal:  Neuroreport       Date:  2007-02-12       Impact factor: 1.837

4.  Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome.

Authors:  Stefano Marenco; Michael A Siuta; J Shane Kippenhan; Samuel Grodofsky; Wei-Li Chang; Philip Kohn; Carolyn B Mervis; Colleen A Morris; Daniel R Weinberger; Andreas Meyer-Lindenberg; Carlo Pierpaoli; Karen Faith Berman
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-07       Impact factor: 11.205

Review 5.  Addressing the Educational Needs of Children with Williams Syndrome: A Rather Neglected Area of Research?

Authors:  Olympia Palikara; Maria Ashworth; Jo Van Herwegen
Journal:  J Autism Dev Disord       Date:  2018-09

Review 6.  Neural phenotypes of common and rare genetic variants.

Authors:  Carrie E Bearden; David C Glahn; Agatha D Lee; Ming-Chang Chiang; Theo G M van Erp; Tyrone D Cannon; Allan L Reiss; Arthur W Toga; Paul M Thompson
Journal:  Biol Psychol       Date:  2008-02-23       Impact factor: 3.251

Review 7.  Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.

Authors:  Daniel Paul Eisenberg; Mbemba Jabbi; Karen Faith Berman
Journal:  Neuroimage       Date:  2010-03-03       Impact factor: 6.556

8.  Genetic influences on sociability: heightened amygdala reactivity and event-related responses to positive social stimuli in Williams syndrome.

Authors:  Brian W Haas; Debra Mills; Anna Yam; Fumiko Hoeft; Ursula Bellugi; Allan Reiss
Journal:  J Neurosci       Date:  2009-01-28       Impact factor: 6.167

9.  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

10.  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

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