Opsoclonus myoclonus syndrome is a rare neurological disorder that primarily affects children. It is characterized by the presence of rapid, involuntary eye movements (opsoclonus) and sudden, brief muscle contractions (myoclonus). This condition is also known by several other names, including:
Opsoclonus myoclonus syndrome can have a sudden onset and may be accompanied by other symptoms such as irritability, sleep disturbances, and cognitive difficulties. The exact cause of this syndrome is still unknown, but it is believed to involve an autoimmune response triggered by an underlying infection or tumor. Treatment typically involves a combination of immunotherapy, such as corticosteroids or intravenous immunoglobulin, and supportive care to manage symptoms and improve quality of life.