Adult-onset opsoclonus-myoclonus-ataxia syndrome as a manifestation of brazilian lyme disease-like syndrome: a case report and review of literature

Described in 1962, the opsoclonus-myoclonus-ataxia syndrome (OMAS) is a rare, neurologically debilitating disorder with distinct characteristics that may begin in childhood or adult life. Although many cases remain without etiological diagnosis, others are related to neoplasms and infectious disease...

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Detalles Bibliográficos
Autores principales: Lino, Angelina Maria Martins, Spera, Raphael Ribeiro, de Campos, Fernando Peixoto Ferraz, Freitas, Christian Henrique de Andrade, Garcia, Márcio Ricardo Taveira, Lopes, Leonardo da Costa, Prokopowitsch, Aleksander Snioka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2014
Materias:
Article / Clinical Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470562/
https://www.ncbi.nlm.nih.gov/pubmed/28652990
http://dx.doi.org/10.4322/acr.2014.005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470562/
https://www.ncbi.nlm.nih.gov/pubmed/28652990
http://dx.doi.org/10.4322/acr.2014.005

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