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An unusual case of Miller Fisher syndrome presenting with proptosis and chemosis
Miller Fisher syndrome (MFS), a rare variant of Guillan-Barré syndrome, is characterized by ophthalmoplegia, ataxia, and areflexia. In addition to this classic triad, symptoms may include bulbar palsy, weakness, and sensory loss. The anti-GQ1b IgG antibody is a sensitive and specific marker for MFS;...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3335291/ https://ncbi.nlm.nih.gov/pubmed/22499110 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mus.23285 |
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