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 S. A. Newman, MD; N. R. Miller, MD; T. Slamovits, MD; R. M. Burde, MD
Affiliation (SAN) Charlottesville, VA; (NRM) Baltimore, MD; (TS) Pittsburgh, PA; (RMB) St. Louis, MO
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
Date 1982
References Attached
Language eng
Format application/pdf
Type Text
Source 1982 Walsh Proceedings
Relation is Part of 1982 Walsh Session, February 19-20
Collection Neuro-Ophthalmology Virtual Education Library: Walsh Session Annual Meeting Archives: https://novel.utah.edu/Walsh/
Publisher North American Neuro-Ophthalmology Society
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah
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
Setname ehsl_novel_fbw
ID 178464
Reference URL https://collections.lib.utah.edu/ark:/87278/s6n0199j
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