Basit öğe kaydını göster

dc.contributor.authorOzmen, O. Afsin
dc.contributor.authorOzgen, Burce
dc.contributor.authorOzmen, Suay
dc.contributor.authorSennaroglu, Levent
dc.date.accessioned2019-12-10T11:31:15Z
dc.date.available2019-12-10T11:31:15Z
dc.date.issued2010
dc.identifier.issn1308-7649
dc.identifier.urihttps://doi.org/
dc.identifier.urihttp://hdl.handle.net/11655/15869
dc.description.abstractFacial paralysis in a newborn is called congenital facial paralysis (CFP). The major role of the physician is to differentiate the etiology of the facial paralysis whether it is traumatic or developmental. This can be achieved by history and physical examination in some cases, however diagnosis may remain uncertain despite all efforts. We herein report a case of CFP, having a normal computed tomography (CT) of the temporal bone whereas a severely hypoplasic facial nerve was seen on the magnetic resonance imaging (MRI) which helps to determine the congenital etiology.
dc.language.isoen
dc.publisherAves
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectOtorhinolaryngology
dc.titleCongenital Facial Paralysis: Facial Nerve Hypoplasia
dc.typeinfo:eu-repo/semantics/article
dc.relation.journalJournal Of International Advanced Otology
dc.contributor.departmentRadyoloji
dc.identifier.volume6
dc.identifier.issue2
dc.identifier.startpage282
dc.identifier.endpage284
dc.description.indexWoS


Bu öğenin dosyaları:

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster