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Opsoclonus myoclonus syndrome in neuroblastoma a report from a workshop on the dancing eyes syndrome at the advances in neuroblastoma meeting in Genoa, Italy, 2004

✍ Scribed by Katherine K. Matthay; Franz Blaes; Barbara Hero; Dominique Plantaz; Pedro De Alarcon; Wendy G. Mitchell; Michael Pike; Vito Pistoia

Book ID
116333620
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
110 KB
Volume
228
Category
Article
ISSN
0304-3835

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## Abstract ## Background Opsoclonus‐myoclonus‐ataxia (OMA) is a paraneoplastic syndrome that occurs in about 2–3% of all cases of neuroblastoma. The histopathologic characteristics of neuroblastoma tumors associated with this syndrome were evaluated in a series of cases and controls. ## Procedur

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## Abstract ## Background Opsoclonus‐myoclonus‐ataxia (OMA) is a paraneoplastic neurologic syndrome affecting 2–3% of children with neuroblastoma. Although children with OMA and neuroblastoma may have higher survival, many experience a significant amount of late neurologic impairment, which may be