IF201b Temporal Cupping with Dominant Hereditary Optic Atrophy

Update Item Information
Identifier IF2_01b
Title IF201b Temporal Cupping with Dominant Hereditary Optic Atrophy
Creator William F. Hoyt, MD
Affiliation (WFH) Professor Emeritus of Ophthalmology, Neurology and Neurosurgery, University of California, San Francisco, California
Subject Optic Disc Atrophy with Special Features; Atrophy with Cupping; Congenital Dominant Optic Atrophy
Description 1969. Dominant hereditary optic atrophy (Kjer) Pair with IF2_1a. Left eye. Boy with reduced central acuity since childhood. and the temporal nerve fiber layer is thin. Anatomy: Optic disc. Pathology: Dominant hereditary optic atrophy. Disease/ Diagnosis: Dominant hereditary optic atrophy. Clinical: Depressed central vision.
Format image/jpeg
Format Creation Scanned at 2700 ppi on Nikon LS2000 and Nikon 8000 film scanners
Type Image
Source 35mm Kodachrome slide; 8a-b
Relation is Part of group IF2
Collection Neuro-Ophthalmology Virtual Education Library: William F. Hoyt Neuro-Ophthalmology Collection: https://novel.utah.edu/Hoyt/
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 1960. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6q26wpq
Setname ehsl_novel_wfh
ID 189674
Reference URL https://collections.lib.utah.edu/ark:/87278/s6q26wpq
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