Opsoclonus myoclonus syndrome in a two-year-old girl: A case report

Abstract

Opsoclonus Myoclonus Syndrome (OMS) is a rare disease that presents with disturbance in gait, muscle spasms, and irregular eye movements. and whose diagnosis and treatment can be challenging in a resource-constrained setting. This is a report of possibly the first documented childhood OMS in Kenya. The diagnosis is was challenging but successful treatment was achieved in a resource-constrained setting.