| Identifier |
19940301_nanos_sciplatform3_07 |
| Title |
Familial Syndrome of Hemiplegic Migraine and Nystagmus: Chromosomal Defect Localization and Ocular Motility Characteristics |
| Creator |
Elliott, Michael A; Peroutka, Stephen J; May, Eugene F; Welsh, S |
| Subject |
Hemiplegic Migraine; Gaze-Evoked Nystagmus; Familial Hemiplegic Migraine; Autosomal Dominant Disorder |
| Description |
Familial hemiplegic migraine (FHM) is an autosomal dominant disorder characterized by transient hemiplegia during the aura phase of a migraine attack. This disease has recently been mapped to chromosome 19 in two families. Prominent gaze-evoked nystagmus has been anecdotally reported in some individuals affected with this disorder. We studied a three generation family with FHM. Nine family members were examined, seven with a history of hemiplegic migraine, and two without. |
| Language |
eng |
| Format |
application/pdf |
| Format Creation |
application/pdf |
| Type |
Text |
| Source |
1994 North American Neuro-Ophthalmology Society Annual Meeting |
| Relation is Part of |
NANOS 1994: Platform Presentations (Session III) |
| Collection |
Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu |
| Publisher |
Spencer S. Eccles Health Sciences Library, University of Utah |
| Holding Institution |
North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416 |
| Rights Management |
Copyright 1994. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright |
| ARK |
ark:/87278/s6wh5wnx |
| Context URL |
The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/ |
| Contributor Primary |
Moster, Mark L |
| Setname |
ehsl_novel_nam |
| ID |
182793 |
| Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6wh5wnx |
