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  Vol. 105 No. 6, June 1979 TABLE OF CONTENTS
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Usher's Syndrome Type III

Robert J. Gorlin, DDS; Thomas J. Tilsner, MD; Sue Feinstein, MA; Arndt J. Duvall, III, MD

Arch Otolaryngol. 1979;105(6):353-354.


Abstract

• We describe a rare example of Usher's syndrome type III in a 9-year-old boy. This type is characterized by retinitis pigmentosa and progressive sensorineural deafness.

(Arch Otolaryngol 105:353-354, 1979)



Author Affiliations

From the Division of Oral Pathology (Dr Gorlin) and the Department of Otolaryngology (Drs Gorlin, Tilsner, and Duvall), University of Minnesota Hospitals and the Children's Health Center (Ms Feinstein), Minneapolis.


Footnotes

Accepted for publication May 23, 1978.

Reprint requests to Division of Oral Pathology, University of Minnesota, 515 Delaware St SE, Minneapolis, MN 55455 (Dr Gorlin).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Retinal Disease in Usher Syndrome III Caused by Mutations in the Clarin-1 Gene
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Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation
Iannaccone et al.
J. Med. Genet. 2003;40:e118-118.
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Usher Syndrome: A Temporal Bone Report
van Aarem et al.
Arch Otolaryngol Head Neck Surg 1995;121:916-921.
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