Usher syndrome: An otoneurologic study

作者：Claes G. Möller, Lars M Ödkvist, William J. Kimberling, Sandra L. H. Davenport, Ira A. Priluck, Valorie White, Karen Biscone‐Halterman, Patrick E. Brookhouser, Gunnar B. Lund, Timothy J. Grissom · 发表于：The Laryngoscope · 年份：1989 · DOI：10.1288/00005537-198901000-00014 · 被引用次数：126 · 研究领域：Hearing, Cochlea, Tinnitus, Genetics、Vestibular and auditory disorders、Ear Surgery and Otitis Media

Usher syndrome is an autosomal recessive disorder characterized by severe hearing loss or deafness and retinitis pigmentosa. Eleven families with 25 affected members were studied. The test battery included genetic studies, clinical examination, audiological, ophthalmologic, and otoneurological tests, and magnetic resonance imaging. Sixteen affected persons had profound hearing loss or were considered anacusic, with absent bilateral vestibular responses. These patients had varying degrees of retinitis pigmentosa. These 16 patients were considered to have type I Usher syndrome. Nine persons were diagnosed as Usher type II with a moderate to profound hearing loss, normal vestibular function, and retinitis pigmentosa of varying degree. Magnetic resonance imaging was normal in all cases. Otoneurological tests indicated no central nervous system disturbances. The conclusion is that hearing loss and balance problems in Usher syndrome are due to inner ear damage with no evidence of central nervous system disturbances. Furthermore, the ataxia seen in Usher type I is due to a combination of retinitis pigmentosa and bilateral peripheral vestibular deficiency.