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Acta Oto-Laryngologica Volume 120, 2000 - Issue 2
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Research Article

The Role of a Family History in King Kopetzky Syndrome (Obscure Auditory Dysfunction)

Dafydd Stephens, Fei Zhao From the Welsh Hearing Institute, Uni6ersity Hospital of Wales, Cardiff, Wales, and the Department of Mechanical Engineering, Tohuku Uni6ersity, Sendai, Japan
Pages 197-200 | Published online: 08 Jul 2009

References

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  • Saunders GH, Haggard MP. The clinical assessment of "obscure auditory dysfunction" (OAD) 2. Case-control analysis of determining factors. Ear Hear 1989; 13: 241–54.
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  • King K, Stephens D. Auditory and psychological fac-tors in "auditory disability with normal hearing". Scand Audiol 1992; 21: 109–14.
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  • Zhao F, Stephens D. Audioscan notches in patients with King-Kopetzky Syndrome and a family history of hearing impairment. J. Aud. Med 1999; 8: 101–12.
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  • Katz J. The use of staggered spondaic words for assess-ing the integrity of the central auditory nervous system. J Sp Hear Dis 1962; 33: 132–46.
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  • Gorlin RJ, Toriello HV, Cohen MM Jnr. Hereditary hereditary hearing loss and its syndromes. Oxford: Oxford University Press, 1995.
  • Van Camp G, Smith RJH. Hereditary hearing loss. World Wide Web URL. http://dnalab-www.uia.ac.be/ dnalab/hhh/ 1999.

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