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...
Saved in:
Main Authors: | Rosiane Souza Rosse (Author), Maíne Vidal Macedo (Author), Tatiana Guimarães de Noronha (Author), Maria Dolores Salgado Quintans (Author), Alexandre Ribeiro Fernandes (Author) |
---|---|
Format: | Book |
Published: |
Sociedade Brasileira de Pediatria,
2023-06-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Síndrome opsoclonus mioclonus. Experiencia en los últimos 12 años en un hospital terciario
by: María Jiménez Legido, et al.
Published: (2020) -
Cerebellar Ataxia, Opsoclonus, and Neuroblastoma
by: J Gordon Millichap
Published: (1987) -
Neurodevelopmental Outcome of Opsoclonus-Ataxia
by: J Gordon Millichap
Published: (2005) -
Opsoclonus-ataxia syndrome and mature ovarian teratoma in an adolescent
by: Emily M. Webster, et al.
Published: (2020) -
Review of Opsoclonus-Myoclonus Ataxia Syndrome in Pediatric Patients
by: Mandy Hsu, et al.
Published: (2024)