What is Opsoclonus-Myoclonus Syndrome?
Opsoclonus-Myoclonus Syndrome (OMS) is a rare neurological condition characterized by sudden, rapid eye movements (opsoclonus) and involuntary muscle jerks (myoclonus).
It can affect both children and adults, but is more commonly observed in children, often presenting suddenly and progressing rapidly.
Side Effects of Opsoclonus-Myoclonus Syndrome
The symptoms of Opsoclonus-Myoclonus Syndrome can vary widely but typically include:
In severe cases, Opsoclonus-Myoclonus Syndrome can lead to significant disability and affect daily activities, making timely diagnosis and treatment crucial.
How is Opsoclonus-Myoclonus Syndrome Diagnosed?
Diagnosing Opsoclonus-Myoclonus Syndrome involves a thorough evaluation by a neurologist or pediatric neurologist. The diagnosis is based on clinical symptoms and supported by specific tests, which may include:
A definitive diagnosis often involves excluding other possible causes of similar symptoms, such as infections or tumors, through these tests.
Potential Treatment of Opsoclonus-Myoclonus Syndrome
Treatment of Opsoclonus-Myoclonus Syndrome typically involves a multidisciplinary approach, including neurologists, immunologists, and rehabilitation specialists. The goals of treatment are to:
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