Literature DB >> 11683329

Preserved otoacoustic emission in a child with a profound unilateral sensorineural hearing loss.

R Ohwatari1, S Fukuda, E Chida, M Matsumura, T Kuroda, M Kashiwamura, Y Inuyama.   

Abstract

We report a case of profound unilateral sensorineural hearing loss with good response of otoacoustic emission. The patient was a 5-year-old boy. who was diagnosed to have unilateral hearing impairment on pure tone audiometry at the first visit. The affected ear showed the absence of auditory brainstem response; however, its transiently evoked otoacoutic emission and distortion product otoacoustic emission were considered to be normal. These findings indicated that the outer hair cell of cochlea was not impaired and that the impairment should be localized between inner hair cells, primary afferent fiber or its synapses, spiral ganglion of the cochlea and acoustic fiber, or at a combination of these areas. That is, evaluation of otoacoustic emission was useful in determining the region of impairment in sensorineural hearing loss. Further follow-up will be necessary to differentiate the present case from auditory neuropathy.

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Year:  2001        PMID: 11683329     DOI: 10.1016/s0385-8146(01)00063-3

Source DB:  PubMed          Journal:  Auris Nasus Larynx        ISSN: 0385-8146            Impact factor:   1.863


  1 in total

1.  Unilateral auditory neuropathy caused by cochlear nerve deficiency.

Authors:  Cheng Liu; Xingkuan Bu; Feiyun Wu; Guangqian Xing
Journal:  Int J Otolaryngol       Date:  2012-02-28
  1 in total

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