| Identifier |
19940301_nanos_sciplatform3_07 |
| Title |
Familial Syndrome of Hemiplegic Migraine and Nystagmus: Chromosomal Defect Localization and Ocular Motility Characteristics |
| Creator |
Michael A. Elliott, MD; S.J. Peroutka, MD, PhD; S. Welsh, MD, PhD; E. May, MD |
| Affiliation |
Tacoma, Washington |
| 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. |
| Date |
1994-03-01 |
| Language |
eng |
| Format |
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: 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 1994. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright |
| ARK |
ark:/87278/s6wh5wnx |
| Setname |
ehsl_novel_nam |
| ID |
182793 |
| Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6wh5wnx |
