Idiopathic opsoclonus myoclonus syndrome: Case report in a 13-month-old female patient
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Keywords

Opsoclonus-myoclonus syndrome
Children
Ataxia

How to Cite

Daniels-García, M. J., Molinares-Núñez, L. P., Muñoz-Álvarez, N. A., & Barrios-Redondo, K. (2022). Idiopathic opsoclonus myoclonus syndrome: Case report in a 13-month-old female patient. Médicas UIS, 35(2), 41–47. https://doi.org/10.18273/revmed.v35n2-2022004

Abstract

Opsoclonus myoclonus syndrome is a rare neurological entity affecting preschool children. Clinically it is characterized by a classic triad of
opsoclonus, myoclonus, and acute ataxia, with a progressive or even incomplete course. Its etiology can be paraneoplastic, in most cases
in association with neuroblastomas, as well as postinfectious or parainfectious, autoimmune or idiopathic. The goal of treatment is immunomodulation with first-line therapy with intravenous steroids, although it can be associated with relapses and long-term neurological
and behavioral sequelae. The opsoclonus myoclonus syndrome represents a diagnostic challenge in patients with acute ataxia given the
variety of clinical presentations, therefore it is important to have a high diagnostic suspicion to ensure timely treatment and aoid future
sequelae.

https://doi.org/10.18273/revmed.v35n2-2022004
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