Ocular Manifestations of Congenital/Inherited Diseases

Update Item Information
Identifier 94_55
Title Ocular Manifestations of Congenital/Inherited Diseases
Creator Mitchell J. Wolin, MD
Affiliation Greenville Memorial Hospital
Contributing Institution AAO/NANOS - American Academy of Ophthalmology / North American Neuro-Ophthalmology Society
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_54.
Date 1999
Date Digital 2004
Language eng
Format image/jpeg
Type Image
Source AAO/NANOS Clinical neuro-ophthalmology : image collection for ophthalmic practitioners. American Academy of Ophthalmology [electronic resource], [San Francisco, Calif.] : AAO, c1999.
Relation is Part of Case 37
Collection Neuro-Ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Publisher North American Neuro-Ophthalmology Society
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah, 10 N 1900 E SLC, UT 84112-5890
Rights Management Copyright 1999. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6p01774
Setname ehsl_novel_aao_nanos
ID 176799
Reference URL https://collections.lib.utah.edu/ark:/87278/s6p01774
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