• C R Otterstedde, U Spandau, A Blankenagel, W J Kimberling, and C Reisser.
• Department of Otolaryngology-Head and Neck Surgery, University of Heidelberg, Germany.
• Laryngoscope. 2001 Jan 1;111(1):84-6.

ObjectivesUsher's syndrome is an autosomal recessive disorder characterized by sensorineural hearing loss and progressive visual loss secondary to retinitis pigmentosa. Usher's syndrome is both clinically and genetically heterogeneous. Three clinical types are known today.MethodsWe conducted a study on 74 patients with Usher's syndrome, performing complete audiological and neurotological examinations.ResultsTwenty-six patients had total profound hearing loss and retinitis pigmentosa (Usher's syndrome type I), and 48 patients had moderate to severe sensorineural hearing loss and retinitis pigmentosa (Usher's syndrome type II). We identified 9 of the 26 Usher's syndrome patients with profound hearing loss who showed a normal response to bithermal vestibular testing.ConclusionsThe combination of profound hearing loss and normal response to bithermal vestibular testing has not been previously described in Usher's syndrome. Therefore we describe a new subtype of Usher's syndrome type I and suggest a modified clinical classification for Usher's syndrome.

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