Usher Syndromes D052245

Related MeSH Hierarchy (10)

Diseases [C] » Eye Diseases [C11] » Retinal Diseases » Retinal Degeneration » Retinal Dystrophies » Retinitis Pigmentosa » Usher Syndromes

Diseases [C] » Eye Diseases [C11] » Vision Disorders » Blindness » Deaf-Blind Disorders » Usher Syndromes

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.   MeSH

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