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Hyperacusis and Williams syndrome

Published online by Cambridge University Press:  29 June 2007

Ajay Nigam  and
Peter R. Samuel
Ajay Nigam
Affiliation:
Department of Otolaryngology, Royal Infirmary, Sunderland.
Peter R. Samuel*
Affiliation:
Department of Otolaryngology, Royal Infirmary, Sunderland.
*
Mr P.R. Samuel, F.R.C.S.E., Dalkeith Lodge, Aykley Heads Farm, Durham DH1 5AN.
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Abstract

Abnormal sensitivity to environmental sounds is a short-term feature often observed following insertion of grommets. Here we describe a child with this symptom who was found to have Williams syndrome, a condition in which hyperacusis is observed in 95 per cent of patients.

Keywords

Middle ear ventilationHyperacusis
Type
Clinical Records
Information
The Journal of Laryngology & Otology , Volume 108 , Issue 6 , June 1994 , pp. 494 - 496
Copyright
Copyright © JLO (1984) Limited 1994

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References

Arnold, R., Yule, W., Martin, N. (1985) The psychological characteristics of infantile hypercalcaemia: a preliminary investigation. Developmental Medicine and Child Neurology 27: 49–59.CrossRefGoogle ScholarPubMed
Beurin, A. J. (1972) Supravalvular aortic stenosis: a complex syndrome with and without mental retardation. Birth Defects Original Article Series 8(5): 45–46.Google Scholar
Boraz, R. A. (1991) Williams syndrome: review of the literature and report of a rare case. Journal of Dentistry for Children 58: 57–59.Google ScholarPubMed
Colley, A., Thakker, Y., Ward, H., Donnai, D. (1992) Unbalanced 13:18 translocation and Williams syndrome. Journal of Medical Genetics 29: 63–65.CrossRefGoogle Scholar
Holmstrom, G., Almond, G., Temple, K., Taylor, D., Baraister, M. (1990) The iris in Williams syndrome. Archives of Diseases in Childhood 65(9): 987–989.CrossRefGoogle ScholarPubMed
Jones, K. L. (1990) Williams syndrome: an historical perspective of its evolution, natural history and etiology. American Journal of Medical Genetics 6 (suppl.): 89–96.Google ScholarPubMed
Jones, K. L., Smith, D. W. (1975) The Williams elfin facies syndrome: a new perspective. Journal of Paediatrics 86: 718–723.CrossRefGoogle ScholarPubMed
Kelly, J. R., Barr, E. S. (1975) The elfin facies syndrome. Oral Surgery 40: 215–218.Google ScholarPubMed
Klein, A. J., Armstrong, B. L., Greer, M. K., Brown, F. R. (1990) Hyperacusis and otitis media in individuals with Williams syndrome. Journal of Speech and Hearing Disorders 55: 339–344.CrossRefGoogle ScholarPubMed
Meyerson, M. D., Frank, R. A. (1987) Language, speech and hearing in Williams syndrome: intervention approaches and research needs. Developmental Medicine and Child Neurology 29: 258–270.Google ScholarPubMed
Preus, M. (1984) The Williams syndrome: objective definition and diagnosis. Clinical Genetics 25: 422–428.CrossRefGoogle ScholarPubMed
Stewart, R. E., Prescott, G. H. (1976). Oral Facial Genetics, C. V. Mosby, St Louis, pp 636–638.Google Scholar
Udwin, O., Yule, W. (1988). Infantile Hypercalcaemia and Williams Syndrome,Infantile Hypercalcaemia Foundation Limited, London, pp 4–16.Google Scholar
Williams, J. C. P., Barrat-Boyes, B. G., Lowe, J. B. (1961) Supravalvular aortic stenosis. Circulation 24: 1311–1318.CrossRefGoogle ScholarPubMed