Autosomal recessive hereditary disorders characterized by congenital SENSORINEURAL HEARING LOSS and RETINITIS PIGMENTOSA. Genetically and symptomatically heterogeneous, clinical classes include type I, type II, and type III. Their severity, age of onset of retinitis pigmentosa and the degree of vestibular dysfunction are variable.
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Syndrome, Usher — Syndromes, Usher — Usher Syndrome — Usher's Syndrome — Syndrome, Usher's — Ushers Syndrome — Dystrophia Retinae Pigmentosa-Dysostosis Syndrome — Dystrophia Retinae Pigmentosa Dysostosis Syndrome — Graefe-Usher Syndrome — Graefe Usher Syndrome — Syndrome, Graefe-Usher — Hallgren Syndrome — Syndrome, Hallgren — Retinitis Pigmentosa-Deafness Syndrome — Retinitis Pigmentosa Deafness Syndrome — Retinitis Pigmentosa-Deafness Syndromes — Syndrome, Retinitis Pigmentosa-Deafness — Syndromes, Retinitis Pigmentosa-Deafness — Deafness-Retinitis Pigmentosa Syndrome — Deafness Retinitis Pigmentosa Syndrome — Deafness-Retinitis Pigmentosa Syndromes — Pigmentosa Syndromes, Deafness-Retinitis — Syndrome, Deafness-Retinitis Pigmentosa — Syndromes, Deafness-Retinitis Pigmentosa — Usher Syndrome, Type III — Usher Syndrome, Type 3 — Usher Syndrome, Type I — Usher Syndrome, Type 1A — Retinitis Pigmentosa And Congenital Deafness — Usher Syndrome, Type 1 — Usher Syndrome, Type I, French Variety — Usher Syndrome, Type II — Usher Syndrome, Type IId