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Audiological findings in 100 USH2 patients
Authors:Abadie C  Blanchet C  Baux D  Larrieu L  Besnard T  Ravel P  Biboulet R  Hamel C  Malcolm S  Mondain M  Claustres M  Roux A-F
Affiliation:CHU Montpellier, Laboratoire de Génétique Moléculaire CHU Montpellier, Centre National de Référence maladies rares "Affections Sensorielles Génétiques" Inserm, U827 Université Montpellier I CNRS UMR5048, Centre de Biochimie Structurale Inserm U554, Montpellier, F-34000, France Institute of Child Health, University College London, London, UK.
Abstract:Abadie C, Blanchet C, Baux D, Larrieu L, Besnard T, Ravel P, Biboulet R, Hamel C, Malcolm S, Mondain M, Claustres M, Roux A-F. Audiological findings in 100 USH2 patients. Bilateral sensorineural hearing loss (HL), classically described as mild to severe with a typically down-sloping audiometric configuration, is the earliest symptom occurring in Usher syndrome type II (USH2). Audiological findings were analyzed in a total of 100 USH2 patients (92 families) divided into three groups according to the gene involved: 88 USH2A, 10 GPR98 and 2 DFNB31 patients. A fine analysis of audiograms was performed (pure tone average, degree of severity, configuration). The median age of HL diagnosis was 5 years (range 8 months-31 years) although the median age at USH2 diagnosis was 34.5 (range 8-76). Moderate HL was predominant (76%) and a gently down-sloping configuration characterized most audiograms (66%). No statistically significant difference was found between USH2A and GPR98 patients but a tendency was clearly noted for more GPR98 patients to present with severe hearing loss. It is not possible to predict the mutated gene from audiograms.
Keywords:audiograms  genetics  hearing loss  Usher syndrome
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