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Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases
Unal, Murat; Vayisoglu, Yusuf.
  • Unal, Murat; Mersin University. Department of Otorhinolaryngology. Mersin. TR
  • Vayisoglu, Yusuf; Mersin University. Department of Otorhinolaryngology. Mersin. TR
Int. arch. otorhinolaryngol. (Impr.) ; 19(2): 151-155, Apr-Jun/2015. tab, graf
Article Dans Anglais | LILACS | ID: lil-747145
ABSTRACT
Introduction Auditory neuropathy/dyssynchrony (AN/AD) comprises a spectrum of pathology affecting the auditory pathways anywhere from the inner hair cells to the brainstem. It is characterized by an absent or atypical auditory brainstem response (ABR) with preservation of the cochlear microphonics and/or otoacoustic emissions (OAEs). Objective Retrospective analysis of patients with AN/AD. Methods Fifteen patients with AN/AD were included in this study and their records were retrospectively investigated. Results Possible etiology of AN/AD was neonatal hyperbilirubinemia in three patients, family history of hearing loss in three patients, consanguineous marriage in two patients, head trauma in two patients, mental motor retardation in one patient, cerebrovascular disease in one patient, and there was no apparent cause in three patients. Conclusion Otolaryngologists should keep in mind the diagnosis of AN/AD especially in patients complaining of difficulty in hearing and speech and audiological evidence of disassociation between pure tone and speech audiometry. ABR and OAE testing is recommended in these patients for AN/AD diagnosis. .
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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Encéphale / Épigenèse génétique / Transcriptome / Syndrome de Klinefelter Type d'étude: Étude observationnelle / Facteurs de risque Limites du sujet: Femelle / Humains / Mâle langue: Anglais Texte intégral: Int. arch. otorhinolaryngol. (Impr.) Thème du journal: Otolaryngologie Année: 2015 Type: Article Pays d'affiliation: Turquie Institution/Pays d'affiliation: Mersin University/TR

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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Encéphale / Épigenèse génétique / Transcriptome / Syndrome de Klinefelter Type d'étude: Étude observationnelle / Facteurs de risque Limites du sujet: Femelle / Humains / Mâle langue: Anglais Texte intégral: Int. arch. otorhinolaryngol. (Impr.) Thème du journal: Otolaryngologie Année: 2015 Type: Article Pays d'affiliation: Turquie Institution/Pays d'affiliation: Mersin University/TR