Literature DB >> 2329796

Hyperacusis and otitis media in individuals with Williams syndrome.

A J Klein1, B L Armstrong, M K Greer, F R Brown.   

Abstract

Williams syndrome is characterized by cardiac defects, varying degrees of physical and developmental delay, stellate eye pattern, possible elevated serum calcium level, and elfin/pixie facial features. A problem perhaps unique to these children is hyperacusis that can be severe enough to disrupt many routine daily activities. Parental questionnaires were used to determine the prevalence of hyperacusis and otitis media in individuals with Williams syndrome. Prevalences of 95% for hyperacusis and 61% for otitis media were found. This was significantly higher than in the general population. Despite the prevalence of hyperacusis, parents of these children were not counseled about management of the problem. The audiologist may become involved with Williams syndrome patients through hearing assessment and management, parental counseling, and research.

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Year:  1990        PMID: 2329796     DOI: 10.1044/jshd.5502.339

Source DB:  PubMed          Journal:  J Speech Hear Disord        ISSN: 0022-4677


  35 in total

1.  Assessment of the influence of background noise on escape-maintained problem behavior and pain behavior in a child with Williams syndrome.

Authors:  M F O'Reilly; C Lacey; G E Lancioni
Journal:  J Appl Behav Anal       Date:  2000

Review 2.  Dysmorphology demystified.

Authors:  William Reardon; Dian Donnai
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2007-05       Impact factor: 5.747

3.  The long-term effects of auditory training on children with autism.

Authors:  S Bettison
Journal:  J Autism Dev Disord       Date:  1996-06

4.  Noise-induced hearing loss induces loudness intolerance in a rat Active Sound Avoidance Paradigm (ASAP).

Authors:  Senthilvelan Manohar; Jaclyn Spoth; Kelly Radziwon; Benjamin D Auerbach; Richard Salvi
Journal:  Hear Res       Date:  2017-07-08       Impact factor: 3.208

5.  Auditory attraction: activation of visual cortex by music and sound in Williams syndrome.

Authors:  Tricia A Thornton-Wells; Christopher J Cannistraci; Adam W Anderson; Chai-Youn Kim; Mariam Eapen; John C Gore; Randolph Blake; Elisabeth M Dykens
Journal:  Am J Intellect Dev Disabil       Date:  2010-03

6.  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

7.  Alterations in diffusion properties of white matter in Williams syndrome.

Authors:  Lori R Arlinghaus; Tricia A Thornton-Wells; Elisabeth M Dykens; Adam W Anderson
Journal:  Magn Reson Imaging       Date:  2011-09-09       Impact factor: 2.546

8.  Regionally specific increased volume of the amygdala in Williams syndrome: evidence from surface-based modeling.

Authors:  Brian W Haas; Kristen Sheau; Ryan G Kelley; Paul M Thompson; Allan L Reiss
Journal:  Hum Brain Mapp       Date:  2012-11-14       Impact factor: 5.038

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.  Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis.

Authors:  Lin Li; Linhuan Huang; Yanmin Luo; Xuan Huang; Shaobin Lin; Qun Fang
Journal:  Mol Syndromol       Date:  2016-02-02
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