Unilateral Auditory Neuropathy Caused by Cochlear Nerve Deficiency
Objective. To explore possible corelationship between the cochlear nerve deficiency (CND) and unilateral auditory neuropathy (AN). Methods. From a database of 85 patients with unilateral profound sensorineural hearing loss, eight who presented with evoked otoacoustic emissions (EOAEs) or cochlear mi...
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Online Access: | http://dx.doi.org/10.1155/2012/914986 |
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doaj-97f970f29c1e472290acc851af8677692020-11-24T22:36:33ZengHindawi LimitedInternational Journal of Otolaryngology1687-92011687-921X2012-01-01201210.1155/2012/914986914986Unilateral Auditory Neuropathy Caused by Cochlear Nerve DeficiencyCheng Liu0Xingkuan Bu1Feiyun Wu2Guangqian Xing3WHO Collaborating Centre for the Prevention of Deafness and Hearing Impairment, Nanjing Medical University, Nanjing 210029, ChinaWHO Collaborating Centre for the Prevention of Deafness and Hearing Impairment, Nanjing Medical University, Nanjing 210029, ChinaWHO Collaborating Centre for the Prevention of Deafness and Hearing Impairment, Nanjing Medical University, Nanjing 210029, ChinaWHO Collaborating Centre for the Prevention of Deafness and Hearing Impairment, Nanjing Medical University, Nanjing 210029, ChinaObjective. To explore possible corelationship between the cochlear nerve deficiency (CND) and unilateral auditory neuropathy (AN). Methods. From a database of 85 patients with unilateral profound sensorineural hearing loss, eight who presented with evoked otoacoustic emissions (EOAEs) or cochlear microphonic (CM) in the affected ear were diagnosed with unilateral AN. Audiological and radiological records in eight patients with unilateral AN were retrospectively reviewed. Results. Eight cases were diagnosed as having unilateral AN caused by CND. Seven had type “A” tympanogram with normal EOAE in both ears. The other patient had unilateral type “B” tympanogram and absent OAE but CM recorded, consistent with middle ear effusion in the affected ear. For all the ears involved in the study, auditory brainstem responses (ABRs) were either absent or responded to the maximum output and the neural responses from the cochlea were not revealed when viewed by means of the oblique sagittal MRI on the internal auditory canal. Conclusion. Cochlear nerve deficiency can be seen by electrophysiological evidence and may be a significant cause of unilateral AN. Inclined sagittal MRI of the internal auditory canal is recommended for the diagnosis of this disorder.http://dx.doi.org/10.1155/2012/914986 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Cheng Liu Xingkuan Bu Feiyun Wu Guangqian Xing |
spellingShingle |
Cheng Liu Xingkuan Bu Feiyun Wu Guangqian Xing Unilateral Auditory Neuropathy Caused by Cochlear Nerve Deficiency International Journal of Otolaryngology |
author_facet |
Cheng Liu Xingkuan Bu Feiyun Wu Guangqian Xing |
author_sort |
Cheng Liu |
title |
Unilateral Auditory Neuropathy Caused by Cochlear Nerve Deficiency |
title_short |
Unilateral Auditory Neuropathy Caused by Cochlear Nerve Deficiency |
title_full |
Unilateral Auditory Neuropathy Caused by Cochlear Nerve Deficiency |
title_fullStr |
Unilateral Auditory Neuropathy Caused by Cochlear Nerve Deficiency |
title_full_unstemmed |
Unilateral Auditory Neuropathy Caused by Cochlear Nerve Deficiency |
title_sort |
unilateral auditory neuropathy caused by cochlear nerve deficiency |
publisher |
Hindawi Limited |
series |
International Journal of Otolaryngology |
issn |
1687-9201 1687-921X |
publishDate |
2012-01-01 |
description |
Objective. To explore possible corelationship between the cochlear nerve deficiency (CND) and unilateral auditory neuropathy (AN). Methods. From a database of 85 patients with unilateral profound sensorineural hearing loss, eight who presented with evoked otoacoustic emissions (EOAEs) or cochlear microphonic (CM) in the affected ear were diagnosed with unilateral AN. Audiological and radiological records in eight patients with unilateral AN were retrospectively reviewed. Results. Eight cases were diagnosed as having unilateral AN caused by CND. Seven had type “A” tympanogram with normal EOAE in both ears. The other patient had unilateral type “B” tympanogram and absent OAE but CM recorded, consistent with middle ear effusion in the affected ear. For all the ears involved in the study, auditory brainstem responses (ABRs) were either absent or responded to the maximum output and the neural responses from the cochlea were not revealed when viewed by means of the oblique sagittal MRI on the internal auditory canal. Conclusion. Cochlear nerve deficiency can be seen by electrophysiological evidence and may be a significant cause of unilateral AN. Inclined sagittal MRI of the internal auditory canal is recommended for the diagnosis of this disorder. |
url |
http://dx.doi.org/10.1155/2012/914986 |
work_keys_str_mv |
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