Considerations in Diagnosing Usher's Syndrome: RP and Hearing Loss

Author:

Vernon Mccay1234,Boughman Joann A.5234,Annala Linda6234

Affiliation:

1. Department of Psychology/Psychobiology, Western Maryland College.

2. Dept. of Psychology and Psychobiology, Western Maryland College, Westminster, MD 21157.

3. Dept. of Human Genetics, Medical College of Virginia, Richmond, VA 23298.

4. Dept. of Education, Box 44064, Baton Rouge, LA 70804.

5. Department of Human Genetics, Medical College of Virginia.

6. Department of Education.

Abstract

The association of hearing loss and retinitis pigmentosa has been generally recognized as Usher's Syndrome, although variations in the syndrome have not been clearly delineated. The diagnosis of a progressive visual disease in a person with severe hearing impairment has devastating implications for the individual's future. This article reviews findings of this syndrome and suggests strategies for dealing with some of the clinical problems displayed by Ushers Syndrome patients.

Publisher

SAGE Publications

Subject

Rehabilitation,Ophthalmology

Reference19 articles.

1. Increased incidence of abnormal nasal cilia in patients with retinitis pigmentosa

2. Heterogeneity of Retinal Degeneration and Hearing Impairment Syndromes

3. BetticaL. J., KeaneG. E., BergmanM., EdgecombC. F., LotzJ., and GoldbergH. H. Communication—A key to service for deaf-blind men and women. A manual for professional workers. Brooklyn: The Industrial Home for the Blind, 1959, 1, 35–59.

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