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: AAO-NANOS Neuro-Ophthalmology Clinical Collection: https://NOVEL.utah.edu/AAO |
Publisher |
North American Neuro-Ophthalmology Society |
Holding Institution |
Spencer S. Eccles Health Sciences Library, University of Utah |
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 |