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Intravenous immunoglobulin therapy for Miller Fisher syndrome

Masahiro Mori1, Satoshi Kuwabara, Toshio Fukutake

  • 1Department of Neurology, Graduate School of Medicine, Chiba University, Inohana, Chuo-ku, Chiba, Japan. morim@faculty.chiba-u.jp

Neurology
|April 4, 2007
PubMed

We analyzed clinical recovery of 92 patients with Miller Fisher syndrome who had been treated with IV immunoglobulin (IVIg; n = 28), plasmapheresis (n = 23), and no immune treatment (n = 41). IVIg slightly hastened the amelioration of ophthalmoplegia and ataxia, but the times of the disappearances of those symptoms were similar among three groups. In Miller Fisher syndrome, IVIg and plasmapheresis seem not to have influenced patients' outcomes, presumably because of good natural recovery.

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