| Literature DB >> 2715696 |
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.Entities:
Mesh:
Year: 1989 PMID: 2715696 DOI: 10.1017/s0022215100109077
Source DB: PubMed Journal: J Laryngol Otol ISSN: 0022-2151 Impact factor: 1.469