Identifier |
69_Retinitis Pigmentosa |
Title |
Retinitis Pigmentosa |
Creator |
David G. Cogan, MD (1908-1993) |
Contributors |
David D. Donaldson |
Affiliation |
(DGC) Former Director of Ophthalmology, National Eye Institute, National Institutes of Health, U.S. Department of Health and Human Services |
Subject |
Retina; Genetic Diseases, Inborn; Neuronal Ceroid-Lipofuscinoses; Refsum Disease; Retinitis Pigmentosa; Retinal Artery; Optic Disc; Fundus Oculi |
Description |
Presenting Symptom: Visual field constriction. Pathology: Pigmentary retinopathy. Clinical: Although occurring usually as a solitary entity, retinitis pigmentosa may be associated with several systemic hereditary conditions: deafness, cerebellar dysfunction, cerebral dysfunction (Vogt-Spielmeyer disease) or Refsum's disease, where the body accumulates excessive amounts of phytanic acid. Characteristic of retinitis pigmentosa is progressive constriction of the visual field, formation of bone corpuscle-like pigmentation in the retina and severe narrowing of the retinal arteries. The pigmentation and narrow arteries are shown on the nasal side of the disc in the present case which was one of solitary retinitis pigmentosa. Disease/ Diagnosis: Retinitis pigmentosa |
Date |
1971 |
Language |
eng |
Format |
image/jpeg |
Type |
Image |
Relation is Part of |
Ocular Fundus Slides |
Collection |
Neuro-Ophthalmology Virtual Education Library: David G. Cogan Collection: https://novel.utah.edu/Cogan/ |
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/s6v40ww2 |
Setname |
ehsl_novel_dgc |
ID |
177325 |
Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6v40ww2 |