Literature DB >> 2118772

Hypothesis for development of a behavioral phenotype in Williams syndrome.

C V Dilts1, C A Morris, C O Leonard.   

Abstract

We investigated the natural history of Williams syndrome (WS), including physical characteristics and cognitive, academic language, sensory integration, and adaptive and maladaptive behavior in 32 patients (age 3 to 30 years). These patients were available for psychoeducational testing, parent interview, medical and educational record review, and behavioral observation. Thirty-seven nonlocal individuals (age 8 months to 31 years) were not tested but data on history and development, sensory integration, adaptive and maladaptive behavior were collected resulting in a total sample of 69. The unique constellation of physical manifestations and associated clinical problems in WS contributes to a characteristic behavioral phenotype of 6 factors beginning in infancy with development of salient attachment behaviors. Later a key issue affecting the learning abilities of both the school-aged child and adult with WS was an inadequate development in the use of tools. Theoretical constructs from developmental behavioral genetics, attachment theory, operant conditioning, neuropsychology, and psychosocial theory considered interactively offer explanations for these characteristics.

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Mesh:

Year:  1990        PMID: 2118772     DOI: 10.1002/ajmg.1320370622

Source DB:  PubMed          Journal:  Am J Med Genet Suppl        ISSN: 1040-3787


  21 in total

Review 1.  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

2.  First principles of Hamiltonian medicine.

Authors:  Bernard Crespi; Kevin Foster; Francisco Úbeda
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2014-03-31       Impact factor: 6.237

3.  A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23.

Authors:  R Peoples; Y Franke; Y K Wang; L Pérez-Jurado; T Paperna; M Cisco; U Francke
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

4.  Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome.

Authors:  L R Osborne; S Soder; X M Shi; B Pober; T Costa; S W Scherer; L C Tsui
Journal:  Am J Hum Genet       Date:  1997-08       Impact factor: 11.025

5.  Behavioural phenotypes and family stress in three mental retardation syndromes.

Authors:  K Sarimski
Journal:  Eur Child Adolesc Psychiatry       Date:  1997-03       Impact factor: 4.785

6.  Second-order belief attribution in Williams syndrome: intact or impaired?

Authors:  K Sullivan; H Tager-Flusberg
Journal:  Am J Ment Retard       Date:  1999-11

7.  Brief report: four case histories and a literature review of Williams syndrome and autistic behavior.

Authors:  C Gillberg; P Rasmussen
Journal:  J Autism Dev Disord       Date:  1994-06

8.  Sensory modulation impairments in children with Williams syndrome.

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

9.  Expecting the worst: observations of reactivity to sound in young children with Williams syndrome.

Authors:  Frank J Gallo; Bonita P Klein-Tasman; Michael S Gaffrey; Phillip Curran
Journal:  Res Dev Disabil       Date:  2007-11-26

10.  Referential communication skills of children with Williams syndrome: understanding when messages are not adequate.

Authors:  Angela E John; Melissa L Rowe; Carolyn B Mervis
Journal:  Am J Intellect Dev Disabil       Date:  2009-03
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