Familial Miller Fisher syndrome

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Miller Fisher syndrome is an acute inflammatory polyradiculoneuropathy that is generally considered a variant of Guillain-Barré syndrome and is characterized by the clinical triad of ataxia, areflexia, and ophthalmoplegia. Several reports of familial Guillain-Barré syndrome have been reported, indicating a possible underlying genetic and/or environmental predisposition to the development of Guillain-Barré syndrome. A familial association in Miller Fisher syndrome has not previously been described in the literature. We report 2 cases of Miller Fisher syndrome presenting simultaneously in siblings, with a review of recent relevant literature.

Original languageEnglish (US)
Pages (from-to)645-648
Number of pages4
JournalJournal of Child Neurology
Volume26
Issue number5
DOIs
StatePublished - May 1 2011

Fingerprint

Miller Fisher Syndrome
Ophthalmoplegia
Guillain-Barre Syndrome
Ataxia

Keywords

  • GQ1b ganglioside
  • Guillain-Barré syndrome
  • Miller Fisher syndrome
  • polyradiculoneuropathy

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

Cite this

Familial Miller Fisher syndrome. / Peeples, Eric S.

In: Journal of Child Neurology, Vol. 26, No. 5, 01.05.2011, p. 645-648.

Research output: Contribution to journalArticle

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