| Identifier |
20090224_nanos_posters_060.pdf |
| Title |
Clinical Characteristics of Patients with Spinocerebellar Ataxia 7 |
| Creator |
Randee Miller; Gregory Van Stavern |
| Affiliation |
(RM) (GVS) Wayne State University, Detroit, MI |
| Subject |
Spinocerebellar Ataxia; Cone-Rod Dystrophy; CAG Trinucleotide Repeats |
| Description |
Spinocerebellar ataxia type 7 (SCA7) is a rare autosomal dominantly inherited neurodegenerative disorder. It is due to abnormal CAG trinucleotide repeat expansion. SCA7 is the only inherited ataxia invariably associated with a cone-rod dystrophy. The clinical course of SCA7 is variable and can initially present with symptoms of ataxia, visual problems, or a combination of the two. |
| Date |
2009-02-24 |
| Language |
eng |
| Format |
application/pdf |
| Type |
Text |
| Source |
2009 North American Neuro-Ophthalmology Society Annual Meeting |
| Relation is Part of |
NANOS 2009: Poster Presentations |
| Collection |
Neuro-Ophthalmology Virtual Education Library: NANOS Annual Meeting Collection: https://novel.utah.edu/collection/nanos-annual-meeting-collection/ |
| Publisher |
North American Neuro-Ophthalmology Society |
| Holding Institution |
Spencer S. Eccles Health Sciences Library, University of Utah |
| Rights Management |
Copyright 2010. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright |
| ARK |
ark:/87278/s6642w3m |
| Setname |
ehsl_novel_nam |
| ID |
180608 |
| Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6642w3m |
