• KSCN
  • KSPAD
  • KSND
  • Contact us
  • E-Submission
ABOUT
BROWSE ARTICLES
EDITORIAL POLICY
FOR CONTRIBUTORS

Articles

Page Path

Case Report

Miller Fisher syndrome mimicking Wernicke encephalopathy during pregnancy

Jung Hwa Seo1orcid , Mi-Ri Kang1orcid , Byeol-A Yoon2orcid , Ki-Hwan Ji1orcid , Seong-il Oh1orcid
Annals of Clinical Neurophysiology 2019;21(1):53-56.
Published online: January 29, 2019
1Department of Neurology, Busan Paik Hospital, Inje University College of Medicine, Busan, Korea
2Department of Neurology, Dong-A University Hospital, Dong-A University College of Medicine, Busan, Korea
Corresponding author:  Seong-il Oh, Tel: +82-51-890-6130, Fax: +82-51-892-8811, 
Email: seongil.oh@gmail.com
Received: 12 June 2018   • Revised: 13 October 2018   • Accepted: 23 October 2018
  • 2,476 Views
  • 73 Download
  • 1 Crossref
  • 0 Scopus
prev next

Miller Fisher syndrome (MFS) is characterized by ataxia, areflexia, and ophthalmoparesis. Here we present a case of MFS mimicking Wernicke encephalopathy (WE) during pregnancy. A 31-year-old woman at 8 weeks of gestation presented with diplopia and ataxia after experiencing nausea and vomiting for several weeks. We initiated thiamine based on a suspicion of WE, which produced no clear effects. However, her symptoms began to improve following intravenous immunoglobulin treatment, and other findings finally lead to a diagnosis of MFS. Because ataxia and ophthalmoparesis can be misdiagnosed as WE during pregnancy, clinicians should consider MFS in the differential diagnosis.

TOP