Literature DB >> 10718438

Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation.

R J Admiraal1, H G Brunner, T L Dijkstra, P L Huygen, C W Cremers.   

Abstract

OBJECTIVE: Evaluation of hearing impairment as a feature of the nonocular Stickler syndrome (type II) linked to COL11A2. STUDY
DESIGN: Family study.
METHODS: General, orthopaedic, ophthalmologic, and otorhinolaryngologic examinations were performed on 15 affected persons in a Dutch family. Audiograms were obtained and/or retrieved from elsewhere. Cross-sectional and longitudinal analyses were conducted on the hearing threshold (sensorineural component) in relation to the patient's age to evaluate whether hearing impairment was progressive.
RESULTS: Mixed hearing loss, i.e., including a substantial air-bone gap of up to 20 to 60 dB, was present in six cases, concomitantly with a submucous or overt cleft palate in five of them. The audiograms in 14 evaluable cases showed the following types of threshold: U-shaped (n = 3), flat (n = 2), flat or gently (downward) sloping (n = 3), gently sloping (n = 3), or steeply sloping (n = 3). Cross-sectional analysis did not reveal any significant effect of age on sensorineural hearing impairment.
CONCLUSION: In contrast to the classic Stickler syndrome (type I) with high myopia, this nonocular type shows a high prevalence of sensorineural hearing impairment. The mean sensorineural hearing threshold in our patients was about 40 dB HL (95% CI, 15-65 dB) and was liable to increase (presumably by presbycusis) by several tens of decibels at the highest frequencies. Given the tendency for otitis media to develop in many of these patients, appropriate otologic care is of major importance.

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Year:  2000        PMID: 10718438     DOI: 10.1097/00005537-200003000-00025

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  6 in total

1.  Audiological findings in otospondylomegaepiphyseal dysplasia (OSMED) associated with a novel mutation in COL11A2.

Authors:  Suna Tokgöz-Yılmaz; Sanem Sahlı; Suat Fitoz; Gonca Sennaroğlu; Mustafa Tekin
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2011-01-03       Impact factor: 1.675

2.  Auditory phenotype in Stickler syndrome: results of audiometric analysis in 20 patients.

Authors:  Frederic R Acke; Freya K Swinnen; Fransiska Malfait; Ingeborg J Dhooge; Els M R De Leenheer
Journal:  Eur Arch Otorhinolaryngol       Date:  2016-01-19       Impact factor: 2.503

3.  A novel retinoic acid-response element requires an enhancer element mediator for transcriptional activation.

Authors:  Laura R Harris; Olli-Pekka Kamarainen; Minna Sevakivi; Gwen C Miller; James W Clarke; Jennifer L Potter; Laura C Bridgewater
Journal:  Biochem J       Date:  2004-10-01       Impact factor: 3.857

Review 4.  Hearing Loss in Stickler Syndrome: An Update.

Authors:  Frederic R E Acke; Els M R De Leenheer
Journal:  Genes (Basel)       Date:  2022-09-01       Impact factor: 4.141

Review 5.  Hearing impairment in Stickler syndrome: a systematic review.

Authors:  Frederic R E Acke; Ingeborg J M Dhooge; Fransiska Malfait; Els M R De Leenheer
Journal:  Orphanet J Rare Dis       Date:  2012-10-30       Impact factor: 4.123

6.  Mutation Spectrum and De Novo Mutation Analysis in Stickler Syndrome Patients with High Myopia or Retinal Detachment.

Authors:  Li Huang; Chonglin Chen; Zhirong Wang; Limei Sun; Songshan Li; Ting Zhang; Xiaoling Luo; Xiaoyan Ding
Journal:  Genes (Basel)       Date:  2020-08-03       Impact factor: 4.096

  6 in total

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