Usher Syndromes


Deafness Retinitis Pigmentosa Syndrome

Deafness-Retinitis Pigmentosa Syndrome

Deafness-Retinitis Pigmentosa Syndromes

Dystrophia Retinae Pigmentosa Dysostosis Syndrome

Dystrophia Retinae Pigmentosa-Dysostosis Syndrome

Graefe Usher Syndrome

Graefe-Usher Syndrome

Hallgren Syndrome

Pigmentosa Syndromes, Deafness-Retinitis

Retinitis Pigmentosa And Congenital Deafness

Retinitis Pigmentosa Deafness Syndrome

Retinitis Pigmentosa-Deafness Syndrome

Retinitis Pigmentosa-Deafness Syndromes

Syndrome, Deafness-Retinitis Pigmentosa

Syndrome, Graefe-Usher

Syndrome, Hallgren

Syndrome, Retinitis Pigmentosa-Deafness

Syndrome, Usher

Syndrome, Usher's

Syndromes, Deafness-Retinitis Pigmentosa

Syndromes, Retinitis Pigmentosa-Deafness

Syndromes, Usher

Usher Syndrome

Usher Syndrome, Type 1

Usher Syndrome, Type 1A

Usher Syndrome, Type 3

Usher Syndrome, Type I

Usher Syndrome, Type I, French Variety

Usher Syndrome, Type II

Usher Syndrome, Type III

Usher Syndrome, Type IId

Usher's Syndrome

Ushers Syndrome

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.