Literature DB >> 8572127

Air-bone gap in patients with X-linked stapes gusher syndrome.

A F Snik1, G C Hombergen, E A Mylanus, C W Cremers.   

Abstract

It is often possible to elicit the stapedius reflex in patients suffering from recessive X-linked progressive mixed deafness syndrome with stapes gusher. The presence of an air-bone gap in the audiogram and the ability to elicit the stapedius reflex are conflicting. Measurements were performed on two patients who were suffering from this syndrome, to establish whether the hearing loss was of the mixed or purely sensorineural type. It was argued that, owing to congenital malformations, the audiovestibular system might act as a more than normally efficient transducer, to convert skull vibrations into inner ear fluid motions, leading to bone conduction thresholds that are better than expected. The results of tone and speech audiometry, stapedius reflex measurements, and brainstem evoked response audiometry in this study showed a pattern similar to that generally seen in patients with purely sensorineural hearing loss. This supports the hypothesis that the air-bone gap in the audiogram does not have the usual significance of a conductive hearing loss component.

Entities:  

Mesh:

Year:  1995        PMID: 8572127

Source DB:  PubMed          Journal:  Am J Otol        ISSN: 0192-9763


  5 in total

Review 1.  Conductive hearing loss caused by third-window lesions of the inner ear.

Authors:  Saumil N Merchant; John J Rosowski
Journal:  Otol Neurotol       Date:  2008-04       Impact factor: 2.311

2.  Audiological and surgical evidence for the presence of a third window effect for the conductive hearing loss in DFNX2 deafness irrespective of types of mutations.

Authors:  Byung Yoon Choi; Yong-Hwi An; Joo Hyun Park; Jeong Hun Jang; Hyun Chung Chung; Ah-Reum Kim; Jun Ho Lee; Chong-Sun Kim; Seung Ha Oh; Sun O Chang
Journal:  Eur Arch Otorhinolaryngol       Date:  2013-02-12       Impact factor: 2.503

3.  A New Pathogenic Variant in POU3F4 Causing Deafness Due to an Incomplete Partition of the Cochlea Paved the Way for Innovative Surgery.

Authors:  Ahmet M Tekin; Marco Matulic; Wim Wuyts; Masoud Zoka Assadi; Griet Mertens; Vincent van Rompaey; Yongxin Li; Paul van de Heyning; Vedat Topsakal
Journal:  Genes (Basel)       Date:  2021-04-21       Impact factor: 4.096

4.  Pou3f4-mediated regulation of ephrin-b2 controls temporal bone development in the mouse.

Authors:  Steven Raft; Thomas M Coate; Matthew W Kelley; E Bryan Crenshaw; Doris K Wu
Journal:  PLoS One       Date:  2014-10-09       Impact factor: 3.240

5.  A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family.

Authors:  Wan Du; Ming-Kun Han; Da-Yong Wang; Bing Han; Liang Zong; Lan Lan; Ju Yang; Qi Shen; Lin-Yi Xie; Lan Yu; Jing Guan; Qiu-Ju Wang
Journal:  Chin Med J (Engl)       Date:  2017-01-05       Impact factor: 2.628

  5 in total

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