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      Miller Fisher syndrome with negative anti-GQ1b immunoglobulin G antibodies.

      Pediatric neurology
      Child, Preschool, Female, Gangliosides, blood, immunology, Humans, Immunoglobulin G, Miller Fisher Syndrome, diagnosis

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          Abstract

          Miller Fisher syndrome is characterized by a triad of ataxia, ophthalmoplegia, and reduced or absent tendon reflexes, with minimal if any limb weakness. Anti-GQ1b immunoglobulin G antibodies are present in high titers in most patients. Presented is a two-year-old female with Miller Fisher syndrome whose blood serum was negative for anti-GQ1b immunoglobulin G antibodies.

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