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From the Department of Neurology (D.T.H., R.S., N.Z.), Childrens National Medical Center; and Department of Neurology (B.E.), Georgetown University Hospital, Washington, DC.
Address correspondence and reprint requests to Dr. David T. Hsieh, Fellow, Department of Neurology, Childrens National Medical Center, 111 Michigan Ave, NW, Washington, DC 20010 dhsieh{at}cnmc.org
An 8-year-old boy developed near complete ophthalmoplegia (video and figure 1), sparing the pupils, with mild gait ataxia, and areflexia. Miller Fisher syndrome was diagnosed after high titers of anti-GQ1b IgG, which are highly disease specific,1 were found in the serum. Nerve conduction, laboratory, and Tensilon testing was not suggestive of alternative diagnoses. MRI in Miller Fisher can show cranial nerve enhancement,2 and in this patient revealed bilateral gadolinium enhancement of cranial nerve III (figure 2). IVIg was given with improvement seen within days. We present a case of near complete ophthalmoplegia from Miller Fisher with video and MRI correlation.
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Supplemental data at www.neurology.org
Disclosure: The authors report no disclosures.
Disclaimer: The views expressed in this article are those of the authors and do not reflect the official policy or position of the United States Air Force, Department of Defense, or the US Government.
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