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Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases

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 a...

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Detalles Bibliográficos
Autores principales: Unal, Murat, Vayisoglu, Yusuf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Publicações Ltda 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399183/
https://www.ncbi.nlm.nih.gov/pubmed/25992171
http://dx.doi.org/10.1055/s-0034-1390328
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author Unal, Murat
Vayisoglu, Yusuf
author_facet Unal, Murat
Vayisoglu, Yusuf
author_sort Unal, Murat
collection PubMed
description 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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spelling pubmed-43991832015-05-19 Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases Unal, Murat Vayisoglu, Yusuf Int Arch Otorhinolaryngol Article 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. Thieme Publicações Ltda 2014-11-28 2015-04 /pmc/articles/PMC4399183/ /pubmed/25992171 http://dx.doi.org/10.1055/s-0034-1390328 Text en © Thieme Medical Publishers
spellingShingle Article
Unal, Murat
Vayisoglu, Yusuf
Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases
title Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases
title_full Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases
title_fullStr Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases
title_full_unstemmed Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases
title_short Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases
title_sort auditory neuropathy/dyssynchrony: a retrospective analysis of 15 cases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399183/
https://www.ncbi.nlm.nih.gov/pubmed/25992171
http://dx.doi.org/10.1055/s-0034-1390328
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