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This document describes the case of a 23 month old male presenting with acute ataxia. His symptoms started two days prior with shaking and difficulty moving. His examination revealed notable truncal and appendicular ataxia. Initial workup was unremarkable. His symptoms progressed to include opsoclonus, leading to a diagnosis of Opsoclonus Myoclonus Ataxia, an autoimmune condition. He received immunomodulating treatment and his symptoms showed significant improvement, though he remains behind on milestones.

Author

Emily Eresuma

Language

EN