| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5590741 | Multiple Sclerosis and Related Disorders | 2017 | 7 Pages |
Abstract
We describe a 19 years old woman with left Horner syndrome (HS), who was diagnosed as NMO with characteristic longitudinally extensive myelitis and positive serum aquaporin-4 immunoglobulin G antibodies (AQP4-IgG). Our report describes one of the very rare ocular motor symptoms in NMO patients.
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Authors
Ä°rem Fatma UludaÄ, Alp Sarıteke, Levent Ãcek, YaÅar Zorlu, Ufuk Åener, Figen TokuçoÄlu, Burhanettin UludaÄ,