Ocular Manifestations of Congenital/Inherited Diseases

Update item information
Identifier 94_54
Title Ocular Manifestations of Congenital/Inherited Diseases
Subject Olivopontocerebellar Degeneration
Description Patients with olivopontocerebellar atrophy may exhibit signs of ocular motor deficits, such as ocular motor apraxia or cerebellar eye signs, and peripheral pigmentary retinopathy and optic atrophy. Pair with 94_55.
Creator AAO/NANOS - American Academy of Ophthalmology / North American Neuro-Ophthalmology Society
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Type Image
Format image/jpeg
Relation is Part of Case 37
Rights Management Copyright 2002. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Contributor Primary Mitchell J. Wolin, MD, Greenville Memorial Hospital
Source AAO/NANOS Clinical neuro-ophthalmology : image collection for ophthalmic practitioners. American Academy of Ophthalmology [electronic resource], [San Francisco, Calif.] : AAO, c1999.
ARK ark:/87278/s6sr2000
Setname ehsl_novel_aao_nanos
Date Created 2004-11-17
Date Modified 2021-05-06
ID 176798
Reference URL https://collections.lib.utah.edu/ark:/87278/s6sr2000
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