Literature DB >> 3601523

Williams syndrome: features in late childhood and adolescence.

R A Pagon, F C Bennett, B LaVeck, K B Stewart, J Johnson.   

Abstract

Nine children with the Williams syndrome were evaluated for physical, neurodevelopmental, and behavioral characteristics to record the natural history of this disorder. The study subjects, who ranged in age from 10 years to 20 years, generally showed lower than expected cognitive functioning with four of the nine functioning in the severely retarded range. However, all the children showed uneven developmental profiles, compared to measured IQ, with reading abilities exceeding the expected level and visual-motor skills deficient for overall performance expectations. All but one child had evidence of supravalvular aortic stenosis on echocardiography, but there was little morbidity from cardiovascular disease in this group of patients. Although all had grown at or below the fifth percentile in early childhood, seven now were above the fifth percentile for height. Personality attributes that characterize younger children with Williams syndrome persisted in this group of older children.

Entities:  

Mesh:

Year:  1987        PMID: 3601523

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  12 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.  Radio-ulnar synostosis in Williams syndrome. A frequently associated anomaly.

Authors:  K A Charvat; L Hornstein; A E Oestreich
Journal:  Pediatr Radiol       Date:  1991

3.  Social Attention, Joint Attention and Sustained Attention in Autism Spectrum Disorder and Williams Syndrome: Convergences and Divergences.

Authors:  Giacomo Vivanti; Peter A J Fanning; Darren R Hocking; Stephanie Sievers; Cheryl Dissanayake
Journal:  J Autism Dev Disord       Date:  2017-06

4.  The iris in Williams syndrome.

Authors:  G Holmström; G Almond; K Temple; D Taylor; M Baraitser
Journal:  Arch Dis Child       Date:  1990-09       Impact factor: 3.791

5.  Behavioral Profiles of Children With Williams Syndrome From Spain and the United States: Cross-Cultural Similarities and Differences.

Authors:  Débora Pérez-García; Carme Brun-Gasca; Luis A Pérez-Jurado; Carolyn B Mervis
Journal:  Am J Intellect Dev Disabil       Date:  2017-03

6.  Language and Literacy Development of Children with Williams Syndrome.

Authors:  Carolyn B Mervis
Journal:  Top Lang Disord       Date:  2009-04

7.  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

8.  Statural growth in Williams-Beuren syndrome.

Authors:  R Pankau; C J Partsch; A Gosch; H C Oppermann; A Wessel
Journal:  Eur J Pediatr       Date:  1992-10       Impact factor: 3.183

9.  The calcitonin-CGRP gene in the infantile hypercalcaemia/Williams-Beuren syndrome.

Authors:  G A Hitman; L Garde; W Daoud; G J Snodgrass
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

10.  Spelling abilities of school-aged children with Williams syndrome.

Authors:  Caroline Greiner de Magalhães; Cláudia Cardoso-Martins; Carolyn B Mervis
Journal:  Res Dev Disabil       Date:  2021-12-04
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