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Klippel-Feil syndrome and hearing loss

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dc.contributor.authorsKoc A., Tutkun A., Batman C., Uneri C., Sehltoglu M.A.
dc.date.accessioned2022-03-28T14:50:09Z
dc.date.accessioned2026-01-11T17:13:13Z
dc.date.available2022-03-28T14:50:09Z
dc.date.issued1996
dc.description.abstractA wide variety of anomalies of the middle and inner ear has been reported in association with congenital deafness in Klippel-Feil syndrome. This syndrome is usually associated with sensorineural hearing loss. Conductive or mixed type hearing losses are rare. In this article this rare clinical entity and our case is discussed.
dc.identifier.issn10191941
dc.identifier.urihttps://hdl.handle.net/11424/255340
dc.language.isoeng
dc.relation.ispartofMarmara Medical Journal
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectHearing loss
dc.subjectKlippel-Feil
dc.subjectSensorineural
dc.titleKlippel-Feil syndrome and hearing loss
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage194
oaire.citation.issue4
oaire.citation.startPage192
oaire.citation.titleMarmara Medical Journal
oaire.citation.volume9

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