Literature DB >> 2338177

A survey of adults with Williams syndrome and idiopathic infantile hypercalcaemia.

O Udwin1.   

Abstract

Questionnaires completed by the caregivers of 119 adults with Williams syndrome or idiopathic infantile hypercalcaemia gave information on current living arrangements, daytime occupations and attainments, self-care skills, social relationships, behavioural and adjustment difficulties and the impact of Williams syndrome and idiopathic infantile hypercalcaemia on caregivers and their families. Many were reported to have marked behavioural and social difficulties persisting into adulthood, and most required some supervision and support in everyday activities such as dressing, toileting and preparing food. Some caregivers were dissatisfied with the level of educational attainment, current daytime occupations and support received from professionals. Over half were concerned about future living arrangements and daytime occupations. Comparisons between the questionnaires for the two groups revealed no phenotypical differences in their abilities or behavioural characteristics.

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Year:  1990        PMID: 2338177     DOI: 10.1111/j.1469-8749.1990.tb16912.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  14 in total

1.  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

2.  Developmental and behavioural characteristics of cri du chat syndrome.

Authors:  K M Cornish; J Pigram
Journal:  Arch Dis Child       Date:  1996-11       Impact factor: 3.791

3.  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

4.  Toward a deeper characterization of the social phenotype of Williams syndrome: The association between personality and social drive.

Authors:  Rowena Ng; Anna Järvinen; Ursula Bellugi
Journal:  Res Dev Disabil       Date:  2014-04-29

5.  Interpretation of ambiguous situations: evidence for a dissociation between social and physical threat in williams syndrome.

Authors:  Helen F Dodd; Melanie A Porter
Journal:  J Autism Dev Disord       Date:  2011-03

6.  Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth.

Authors:  L A Pérez Jurado; R Peoples; P Kaplan; B C Hamel; U Francke
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

7.  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

8.  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

9.  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

10.  Long term effects of periconceptional multivitamin supplements for prevention of neural tube defects: a seven to 10 year follow up.

Authors:  M Holmes-Siedle; J Dennis; R H Lindenbaum; A Galliard
Journal:  Arch Dis Child       Date:  1992-12       Impact factor: 3.791

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