Identifier |
wh_ch11_p480_2 |
Title |
Walsh & Hoyt: Autosomal-Dominant Progressive Optic Atrophy with Progressive Hearing Loss and Ataxia (CAPOS Syndrome) |
Creator |
Nancy J. Newman, MD |
Affiliation |
Emory Eye Center |
Subject |
Optic Nerve Diseases; Genetic Diseases, Inborn; Autosomal-Dominant Progressive Optic Atrophy; Progressive Hearing Loss; Ataxia; CAPOS Syndrome |
Description |
In this syndrome, described by Sylvester in 1958, a father and his six children were found to have bilateral optic atrophy and hearing loss, associated with ataxia and limb weakness. The onset of visual loss in these patients was between 2.5 and 9 years of age. The hearing loss was only moderate and, like the optic atrophy, was slowly progressive. The ataxia in these patients primarily affected the legs, withweakness and muscle wasting mainly affecting the shoulder girdle and hands. The relationship of this syndrome to Friedreichs ataxia was discussed in detail by Sylvester. |
Date |
2005 |
Language |
eng |
Format |
application/pdf |
Type |
Text |
Source |
Walsh and Hoyt's Clinical Neuro-Ophthalmology, 6th Edition |
Relation is Part of |
Walsh and Hoyt's Clinical Neuro-Ophthalmology Walsh and Hoyt's Clinical Neuro-Ophthalmology |
Collection |
Neuro-Ophthalmology Virtual Education Library: Walsh and Hoyt Textbook Selections Collection: https://NOVEL.utah.edu |
Publisher |
Wolters Kluwer Health, Philadelphia |
Holding Institution |
Spencer S. Eccles Health Sciences Library, University of Utah |
Rights Management |
Copyright 2005. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright |
ARK |
ark:/87278/s6vx3r35 |
Setname |
ehsl_novel_whts |
ID |
186689 |
Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6vx3r35 |