| Literature DB >> 27928406 |
Deniz Somer1, Arzu Yilmaz2, Serap Tiras Teber3, Fatma Gul Cinar1.
Abstract
Miller Fisher syndrome (MFS) is characterised by the triad of ophthalmoplegia, ataxia, and areflexia. A case with external ophthalmoplegia and absence of ataxia and areflexia until the end of second week is presented. Electrophysiological findings became apparent after the third week and showed reduced amplitudes of sensory nerve action potentials and prolonged latencies of F with no evidence of conduction blocks. There was no response to intravenous immunoglobulin, but there was response to corticosteroids. This case may represent an atypical MFS with late presenting electrophysiological abnormalities. Corticosteroids can be a therapeutic option when intravenous immunoglobulin fails to control clinical symptoms.Entities:
Keywords: Acute esotropia; Miller Fisher syndrome; esotropia; external ophthalmoplegia; ophthalmoplegia
Year: 2016 PMID: 27928406 PMCID: PMC5123134 DOI: 10.1080/01658107.2016.1192197
Source DB: PubMed Journal: Neuroophthalmology ISSN: 0165-8107