Article ID Journal Published Year Pages File Type
3086290 Pediatric Neurology 2008 5 Pages PDF
Abstract

We describe 2 children with postinfectious opsoclonus-myoclonus syndrome. Although the patients initially responded to monotherapy with methylprednisolone, intravenous immunoglobulins, or rituximab, they manifested persistent neurologic deficits and relapsing signs. Treatment with rituximab in combination with intravenous immunoglobulin, however, resulted in significant longterm clinical improvement.

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Life Sciences Neuroscience Developmental Neuroscience
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