Single gene influences on radiologically-detectable malformations of the inner ear

Shelley D Smith, Lee A. Harker

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Inner ear malformations associated with hearing loss or vestibular dysfunction are discussed from the viewpoint of the etiologies of the malformation. Symptoms of classification of inner ear malformations are discussed. The significance of malformations of the cochlea and vestibular aqueduct to auditory function are discussed. Genetics features and characteristics of Branchio-oto-renal, Waardenburg's, Pendred's, DiGeorge's, Wildervanck, Fountain, and Treacher Collins syndromes are discussed in relation to ear abnormalities and hearing. Similar attention is given to genetic studies of nonsyndromic hearing loss.

Original languageEnglish (US)
Pages (from-to)391-410
Number of pages20
JournalJournal of Communication Disorders
Volume31
Issue number5
DOIs
StatePublished - Jan 1 1998

Fingerprint

Inner Ear
Vestibular Aqueduct
Mandibulofacial Dysostosis
Cochlea
etiology
Hearing Loss
Hearing
Genes
Ear
Kidney
Gene
Hearing Impairment
Nonsyndromic Deafness

ASJC Scopus subject areas

  • Experimental and Cognitive Psychology
  • Linguistics and Language
  • Cognitive Neuroscience
  • Speech and Hearing
  • LPN and LVN

Cite this

Single gene influences on radiologically-detectable malformations of the inner ear. / Smith, Shelley D; Harker, Lee A.

In: Journal of Communication Disorders, Vol. 31, No. 5, 01.01.1998, p. 391-410.

Research output: Contribution to journalArticle

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