Literature DB >> 2715696

Wildervanck's syndrome--unilateral Mondini dysplasia identified by computed tomography.

P D West1, A Gholkar, R T Ramsden.   

Abstract

We present a case of the Wildervanck (cervico-oculo-acoustic) syndrome exhibiting congenital deafness. Klippel-Feil anomaly and lateral rectus palsy with enophthalmos. Audiometry indicated a predominantly conductive loss which, because of masking difficulties, was assumed to be bilateral: an erroneous assumption supported by results of conventional petrous bone tomography which failed to demonstrate any abnormality of the inner ears. Computed tomography (CT), however, revealed a severe Mondini dysplasia of one ear, a condition which must be assumed to be associated with severe sensorineural hearing loss. Reconstructive middle ear surgery for the conductive loss on the other side was therefore contraindicated.

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Year:  1989        PMID: 2715696     DOI: 10.1017/s0022215100109077

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN: 0022-2151            Impact factor:   1.469


  2 in total

1.  Audiological abnormalities in the Klippel-Feil syndrome.

Authors:  J M McGaughran; P Kuna; V Das
Journal:  Arch Dis Child       Date:  1998-10       Impact factor: 3.791

2.  X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.

Authors:  C Piussan; A Hanauer; N Dahl; M Mathieu; C Kolski; V Biancalana; S Heyberger; V Strunski
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

  2 in total

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