Neuromyelitis optica presenting with horner syndrome: A case report and review of literature
- PMID: 28619428
- DOI: 10.1016/j.msard.2017.03.011
Neuromyelitis optica presenting with horner syndrome: A case report and review of literature
Abstract
Neuromyelitis optica (NMO) is a demyelinating disease of the central nervous system that predominantly affects the spinal cord and optic nerves. 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.
Keywords: Horner syndrome; Multiple sclerosis; Neuromyelitis optica.
Copyright © 2017 Elsevier B.V. All rights reserved.
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