Dancing eyes-dancing feet syndrome
Other Names for this Disease
- Ataxo-opso-myoclonus syndrome
- Dancing eye syndrome
- Dancing eye-dancing feet syndrome
- Infantile polymyoclonus
- Kinsbourne syndrome
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 OMS typically occurs in association with tumors (neuroblastomas), or following a viral infection. Treatment may include corticosteroids or ACTH (adrenocorticotropic hormone). When there is a tumor present, treatment may include chemotherapy, surgery, and/or radiation. When the underlying cause of OMS is treated, symptoms may improve. Relapses are common and may occur without warning.Dancing eyes-dancing feet syndrome, also known as opsoclonus myoclonus syndrome (OMS), is a rare neurologic disorder characterized by ocular (eye), behavioral, sleep, and language problems. The onset is usually abrupt, often severe, and can become chronic.
Last updated: 4/16/2014
- Pranzatelli MR. Opsoclonus-Myoclonus Syndrome. National Organization for Rare Disorders (NORD). 2009; http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Opsoclonus-Myoclonus%20Syndrome. Accessed 11/2/2009.
- NINDS Opsoclonus Myoclonus Information Page. National Institute of Neurological Disorders and Stroke (NINDS). 2007; http://www.ninds.nih.gov/disorders/opsoclonus_myoclonus/opsoclonus_myoclonus.htm. Accessed 11/2/2009.
- Pranzatelli MR. What is the Opsoclonus-Myoclonus Syndrome?. Opsoclonus-Myoclonus U.S.A. And International web site. http://www.omsusa.org/pranzatelli-Brochure1.htm. Accessed 11/2/2009.
- Marc Tardieu. Opsoclonus-myoclonus syndrome. Orphanet. March, 2006; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=EN&Expert=1183. Accessed 4/16/2014.
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