Journal of Pediatric Neurology 2016; 14(02): 075-077
DOI: 10.1055/s-0036-1584277
Case Report
Georg Thieme Verlag KG Stuttgart · New York

Miller Fisher Syndrome Associated with Parvovirus B19 Infection in a Child

Authors

  • Filippo Greco

    1   Unit of Clinical Pediatrics, Department of Medical and Pediatric Sciences, University of Catania, Catania, Italy
  • Alice Le Pira

    1   Unit of Clinical Pediatrics, Department of Medical and Pediatric Sciences, University of Catania, Catania, Italy
  • Luisa Scalora

    1   Unit of Clinical Pediatrics, Department of Medical and Pediatric Sciences, University of Catania, Catania, Italy
  • Roberta Catania

    1   Unit of Clinical Pediatrics, Department of Medical and Pediatric Sciences, University of Catania, Catania, Italy
  • Tiziana Timpanaro

    1   Unit of Clinical Pediatrics, Department of Medical and Pediatric Sciences, University of Catania, Catania, Italy
  • Pierluigi Smilari

    1   Unit of Clinical Pediatrics, Department of Medical and Pediatric Sciences, University of Catania, Catania, Italy
  • Giovanni Sorge

    1   Unit of Clinical Pediatrics, Department of Medical and Pediatric Sciences, University of Catania, Catania, Italy
Further Information

Publication History

18 September 2015

09 February 2016

Publication Date:
30 May 2016 (online)

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Abstract

Miller Fisher syndrome (MFS) is a variant of Guillain–Barré syndrome, and it is typically characterized by the triad of ophthalmoplegia, ataxia, and areflexia. We report a 13-year-old boy affected with MFS associated with parvovirus B19 infection in which immunoglobulin (Ig)G and IgM anti-GQ1b antibodies were not detected. Treatment with intravenous Igs resulted in a progressive and rapid resolution of the clinical features. To our knowledge, this is the first example in the literature of seronegative anti-GQ1b antibody MFS associated with parvovirus B19 infection in childhood. The possible role of other gangliosides is discussed.