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Long-term outcome in children with opsoclonus-myoclonus and ataxia and coincident neuroblastoma

✍ Scribed by Paul S. Koh; John G. Raffensperger; Sharon Berry; Marianne B. Larsen; Helen S. Johnstone; Pauline Chou; Susan R. Luck; Michael Hammer; Susan L. Cohn

Book ID
117164247
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
462 KB
Volume
125
Category
Article
ISSN
1097-6833

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A retrospective data collection was performed on 29 children diagnosed with neuroblastoma and opsoclonus-myoclonus between 1983-1993 from Pediatric Oncology Group institutions. The aim was to describe neurologic outcome in children with neuroblastoma and opsoclonus-myoclonus. Age at diagnosis ranged

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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