Objective: To evaluate hearing impairment in 2 common genetic subtypes of Usher syndrome, USH1B and USH2A. Design: Cross-sectional analysis of hearing threshold related to age in patients with genotypes determined by linkage and mutation analysis. Setting: Otolaryngology department, university referral center. Patients: Nineteen patients with USH1B and 27 with USH2A were examined. All participants were living in the Netherlands and Belgium. Main Outcome Measure: Pure tone audiometry of the best ear at last visit. Results: The patients with USH1B had residual hearing without age dependence, with minimum thresholds of 80, 95, and 120 dB at 0.25, 0.5, and 1 to 2 kHz, respectively. Mean thresholds of patients with USH2A were about 45 to 55 dB better than these minimum values. Distinctive audiographic features of patients with USH2A were maximum hearing thresholds of 70, 80, and 100 dB at 0.25, 0.5, and 1 kHz, respectively, only at younger than 40 years. Progression of hearing impairment in USH2A was 0.7 dB/y on average for 0.25 to 4 kHz and could not be explained by presbyacusis alone. Conclusions: The USH1B and USH2A can be easily distinguished by hearing impairment at younger than 40 years at the low frequencies. Hearing impairment m our patients with USH2A could be characterized as progressive.
|Original language||English (US)|
|Number of pages||5|
|Journal||Archives of Otolaryngology - Head and Neck Surgery|
|State||Published - Apr 1999|
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