| 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 |
| 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 |
