Opsoclonus is an ocular dyskinesia characterized by involuntary, arrhythmic, multidirectional saccades. In pediatrics, opsoclonus is most commonly attributed to the rare neuroinflammatory disorder opsoclonus‐myoclonus‐ataxia syndrome (OMAS), typically considered a paraneoplastic syndrome associated with neural crest tumors. However, opsoclonus can manifest as a symptom of other disease processes including toxic, metabolic, and genetic etiologies, and there is a paucity of literature focusing on the differential diagnoses and etiologic workup of opsoclonus in children. This review aims to address this knowledge gap with the ultimate goal of providing a schema facilitating the evaluation of a pediatric patient presenting with opsoclonus.
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Reed et al. (2026) studied this question.
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