Literature DB >> 18700423

Hearing impairment in genotyped Wolfram syndrome patients.

Rutger F Plantinga1, Ronald J E Pennings, Patrick L M Huygen, Rocco Bruno, Philipp Eller, Timothy G Barrett, Bernard Vialettes, Veronique Paquis-Fluklinger, Fortunato Lombardo, Cor W R J Cremers.   

Abstract

OBJECTIVES: Wolfram syndrome is a progressive neurodegenerative syndrome characterized by the features "DIDMOAD" (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness). We sought to study the audiometric data of genotyped Wolfram syndrome patients with sensorineural hearing impairment.
METHODS: Pure tone threshold data of 23 Wolfram syndrome patients were used for cross-sectional analysis in subgroups (age less than 16 years or between 19 and 25 years, gender, and origin).
RESULTS: All subgroups, with 1 exception, showed a fairly similar type of hearing impairment with, on average, thresholds of about 25 dB (range, 0 to 65 dB) at 0.25 to 1 kHz, gently sloping downward to about 60 dB (range, 25 to 95 dB) at 8 kHz. The subgroup of Dutch women, which was excluded from the calculations of the average hearing thresholds, showed a higher degree of hearing impairment. Only the latter subgroup showed progression; however, contrary to the previous longitudinal analysis, progression was not significant in the present cross-sectional analysis, presumably because of the high degree of cross-subject variability.
CONCLUSIONS: This unique collection of audiometric data from genotyped Wolfram syndrome patients shows no substantial progression in sensorineural hearing impairment with advancing age, no relation to the types of WFS1 mutations identified, and, with exclusion of the subgroup of Dutch female patients, no significant sex-related differences.

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Year:  2008        PMID: 18700423     DOI: 10.1177/000348940811700704

Source DB:  PubMed          Journal:  Ann Otol Rhinol Laryngol        ISSN: 0003-4894            Impact factor:   1.547


  9 in total

1.  A clinical case study of a Wolfram syndrome-affected family: pattern-reversal visual evoked potentials and electroretinography analysis.

Authors:  Ewa Langwińska-Wośko; Karina Broniek-Kowalik; Kamil Szulborski
Journal:  Doc Ophthalmol       Date:  2012-02-07       Impact factor: 2.379

2.  Wolfram syndrome: a clinicopathologic correlation.

Authors:  Justin B Hilson; Saumil N Merchant; Joe C Adams; Jeffrey T Joseph
Journal:  Acta Neuropathol       Date:  2009-05-16       Impact factor: 17.088

Review 3.  Genetics of hearing and deafness.

Authors:  Simon Angeli; Xi Lin; Xue Zhong Liu
Journal:  Anat Rec (Hoboken)       Date:  2012-10-08       Impact factor: 2.064

4.  Audiologic and vestibular findings in Wolfram syndrome.

Authors:  Roanne K Karzon; Timothy E Hullar
Journal:  Ear Hear       Date:  2013 Nov-Dec       Impact factor: 3.570

Review 5.  Genetics of non syndromic hearing loss.

Authors:  M D Venkatesh; Nikhil Moorchung; Bipin Puri
Journal:  Med J Armed Forces India       Date:  2015-09-26

6.  Diabetes mellitus, diabetes insipidus, optic atrophy, and deafness: A case of Wolfram (DIDMOAD) syndrome.

Authors:  Nasrollah Maleki; Bahman Bashardoust; Anahita Zakeri; Azita Salehifar; Zahra Tavosi
Journal:  J Curr Ophthalmol       Date:  2016-01-02

7.  Longitudinal hearing loss in Wolfram syndrome.

Authors:  Roanne Karzon; Anagha Narayanan; Ling Chen; Judith E C Lieu; Tamara Hershey
Journal:  Orphanet J Rare Dis       Date:  2018-06-27       Impact factor: 4.123

8.  Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1.

Authors:  Barend F T Hogewind; Ronald J E Pennings; Frans A Hol; Henricus P M Kunst; Elisabeth H Hoefsloot; Johannes R M Cruysberg; Cor W R J Cremers
Journal:  Mol Vis       Date:  2010-01-12       Impact factor: 2.367

9.  A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report.

Authors:  Min Li; Jia Liu; Huan Yi; Li Xu; Xiufeng Zhong; Fuhua Peng
Journal:  BMC Pediatr       Date:  2018-03-17       Impact factor: 2.125

  9 in total

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