Identifier |
20230312_nanos_posters_202 |
Title |
Diplopia Due to Congenital Myasthenic Syndrome Mimics Divergence Insufficiency |
Creator |
Yan Yan, MD, PhD |
Affiliation |
(YY) Renji Hospital, Shanghai Jiaotong Univeristy, School of Medicine |
Subject |
Ocular Motility; Genetic Disease; Myasthenia |
Description |
Congenital myasthenic syndromes (CMS) are a genotypically and phenotypically heterogeneous group of neuromuscular disorders from the impaired neuromuscular transmission. Mutations in the AGRN gene manifest phenotypically as either early-onset or late-onset CMS. The late-onset type is characterized by ptosis, ophthalmoparesis, and mild facial and bulbar weakness. We reported a rare case of diplopia due to CMS mimicking divergence insufficiency. |
Date |
2023-03-14 |
Language |
eng |
Format |
application/pdf |
Type |
Text |
Source |
2023 North American Neuro-Ophthalmology Society Annual Meeting |
Relation is Part of |
NANOS Annual Meeting 2023: Poster Session I: Ocular Motility Disorders and Nystagmus |
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 2023. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright |
ARK |
ark:/87278/s6pp7p2e |
Setname |
ehsl_novel_nam |
ID |
2335407 |
Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6pp7p2e |