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 language | English (US) |
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Pages (from-to) | 645-648 |
Number of pages | 4 |
Journal | Journal of Child Neurology |
Volume | 26 |
Issue number | 5 |
DOIs | |
State | Published - May 2011 |
Externally published | Yes |
Keywords
- GQ1b ganglioside
- Guillain-Barré syndrome
- Miller Fisher syndrome
- polyradiculoneuropathy
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Clinical Neurology