Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.16/437
Título: Opsoclonus myoclonus syndrome: how long are we going to go on researching?]
Autor: Ramos, S.
Temudo, T.
Data: Ago-2002
Editora: Cesar Viguera
Resumo: Rev Neurol. 2002 Aug 16-31;35(4):322-5. [Opsoclonus myoclonus syndrome: how long are we going to go on researching?] [Article in Spanish] Ramos S, Temudo T. Interna complementar de Pediatria. Serviço de Pediatria. Hospital Geral de Santo Antonio, Porto, Portugal. teresatemudo@netcabo.pt Abstract INTRODUCTION: Opsoclonus myoclonus is a rare neurological syndrome affecting children and adults, and which is characterised by a sudden onset of chaotic eye movements and myoclonias. In children it generally appears before the age of three as a parainfectious or paraneoplasic process; the type of tumour most frequently associated with this syndrome is the neuroblastoma. CASE REPORT: We report the case of a 22 month old girl who, after a febrile syndrome probably caused by a virus, began to present myoclonias in the upper and lower limbs, opsoclonus, a marked ataxic gait and extreme irritability. After ruling out neoplasia, oral corticotherapy was started and the neurological picture gradually improved. CONCLUSION: By reporting this clinical picture, our intention is to make the particular aspects of this neurological condition known, and highlight the need for neoplasias to be detected in time and for early treatment in order to prevent sequelae, especially when it appears as a paraneoplasic syndrome. PMID: 12235560 [PubMed - indexed for MEDLINE]
URI: http://hdl.handle.net/10400.16/437
ISSN: 0210-0010
Versão do Editor: http://www.revneurol.com/
Aparece nas colecções:SNeuroP - Artigos publicados em revistas indexadas na Medline

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