Acute, Bilateral Visual Loss in a Pediatric Patient

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Title Acute, Bilateral Visual Loss in a Pediatric Patient
Creator Elizabeth H. Roll; Larry P. Frohman; Roger E. Turbin
Affiliation Institute of Ophthalmology and Visual Science, Rutgers New Jersey Medical School, Newark, New Jersey
Abstract This is a case report on a patient who had a 40-year history of gradual vision loss and only recently diagnosed with autosomal dominant optic atrophy (ADOA) secondary to an OPA1 gene mutation. To the best of our knowledge, this is the longest duration between symptoms and diagnosis for a patient with ADOA.
Subject Child; Vision Disorders; Visual Acuity
OCR Text Show
Date 2022-12
Date Digital 2022-12
Language eng
Format application/pdf
Type Text
Publication Type Journal Article
Source Journal of Neuro-Ophthalmology, December 2022, Volume 42, Issue 4
Collection Neuro-Ophthalmology Virtual Education Library: Journal of Neuro-Ophthalmology Archives: https://novel.utah.edu/jno/
Publisher Lippincott, Williams & Wilkins
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah
Rights Management © North American Neuro-Ophthalmology Society
ARK ark:/87278/s6n709yx
Setname ehsl_novel_jno
ID 2392959
Reference URL https://collections.lib.utah.edu/ark:/87278/s6n709yx
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