Mesh term Usher Syndromes
Browse to parent terms:Deaf-Blind Disorders
Hearing Loss, Sensorineural
Retinitis Pigmentosa
Description
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.Search for this term in our Faculty Database
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