Leber's Optic Neuropathy; A Role for Intervention

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Identifier walsh_1982_s4_c2
Title Leber's Optic Neuropathy; A Role for Intervention
Creator Steven A. Newman, MD, University of Virginia School of Medicine
Subject Optic Atrophy, Hereditary, Leber; Optic Disk; Telangiectasis; Scotoma; Gliosis
History Case 1: A 15-year old male with 7-month history of blurred vision OD. Case 2: An 18-year old male with a 1-year history of bilateral loss of vision. Case 3: A 33-year old male with a 2-month history of decreased OS. Case 4: A 10-year old male with a 1-month history of decreased vision OS.
Pathology Maternally-linked genetic disorder presenting as an acute or subacute central vision loss leading to central scotoma and blindness.
Disease/Diagnosis Leber Hereditary Optic Neuropathy
Clinical Case 1 VA: 5/200 OD, 20/400 OS Case 2 VA: 20/400 OU Case 3 VA: Normal vision OD, Decreasing vision OS Case 4: 20/20 OD, 5/200 OS
Presenting Symptom Blurred vision; Central scotoma
Neuroimaging CT
Treatment N/A
References Attached
Language eng
Format application/pdf
Type Text
Source 1982 Walsh Proceedings
Relation is Part of Case presented at the NANOS 1982 Walsh Session, February 19-20 Contributor Primary
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Rights Management Copyright 2008. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6n0199j
Contributor Primary Newman, Steven A.
Contributor Secondary Miller, Neil R.; Slamovits , T.; Burde, R.M.
Setname ehsl_novel_fbw
ID 178464
Reference URL https://collections.lib.utah.edu/ark:/87278/s6n0199j
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