Síndrome opsoclonus-mioclonus-ataxia: relato de caso

Opsoclonus-myoclonus-ataxia syndrome (AOM), also known as Kinsbourne syndrome, is a rare neurological disease in childhood, clinically characterized by rapid, irregular and multidirectional eye movements, myoclonic movements in the trunk, face and / or extremities and ataxia. Irritability and distur...

Szczegółowa specyfikacja

Opis bibliograficzny
Główni autorzy: Rosiane Souza Rosse, Maíne Vidal Macedo, Tatiana Guimarães de Noronha, Maria Dolores Salgado Quintans, Alexandre Ribeiro Fernandes
Format: Artykuł
Język:English
Wydane: Sociedade Brasileira de Pediatria 2023-06-01
Seria:Residência Pediátrica
Hasła przedmiotowe:
Dostęp online:https://residenciapediatrica.com.br/detalhes/1317/sindrome%20opsoclonus-mioclonus-ataxia-%20relato%20de%20caso

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