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Eur J Paediatr Neurol ; 14(2): 156-61, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19423368

RESUMO

The incidence, mode of presentation and management of Dancing Eye Syndrome/Opsoclonus-Myoclonus Syndrome (DES/OMS) was prospectively evaluated in 20 United Kingdom (UK) paediatric neurology centres by questionnaire over a 24-month period between 2003 and 2005. Nineteen children were notified, giving an incidence of 0.18 cases per million total population per year. Mean age at presentation was 18 months (range 3-42 months). Fifteen families consented to participate in the study. Atypical features were present in 6/15 cases including very delayed presentation of opsoclonus, dysphagia, and rapid spontaneous improvement without treatment. Only 4/15 cases were associated with neuroblastoma (NB) but current practice in excluding this is diverse and a standardised approach is suggested.


Assuntos
Síndrome de Opsoclonia-Mioclonia/epidemiologia , Síndrome de Opsoclonia-Mioclonia/terapia , Neoplasias Abdominais/epidemiologia , Neoplasias Abdominais/patologia , Neoplasias Encefálicas/epidemiologia , Neoplasias Encefálicas/patologia , Catecolaminas/urina , Pré-Escolar , Transtornos de Deglutição/epidemiologia , Feminino , Humanos , Incidência , Lactente , Imageamento por Ressonância Magnética , Masculino , Neuroblastoma/epidemiologia , Neuroblastoma/patologia , Síndrome de Opsoclonia-Mioclonia/diagnóstico , Prevalência , Estudos Prospectivos , Remissão Espontânea
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