Epilepsia Rolândica: Uma revisão bibliográfica

Epilepsy is a medical condition in which there is disturbance of brain activity, characterized by focal, unprovoked or reflex seizures. The objective was to discuss the diagnosis and evolution of Rolandic Epilepsy in childhood, syndromic characteristics and pharmacological therapeutic options. Mater...

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Detalles Bibliográficos
Autores: Santos, Mikaellem Nogueira dos, Rezende, Bruna Heduarda de, Nery, Daniela Luiz, Rezende, Fernanda de, Barbosa, Amanda Ferreira, Silva, Laura Vitória de Lima, Sousa, Marciana Gomes de, Amorim Filho , Benedito Domingos
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:Brasil
Institución:Universidade Federal de Itajubá (UNIFEI)
Repositorio:Research, Society and Development
Idioma:portugués
OAI Identifier:oai:ojs.pkp.sfu.ca:article/45079
Acceso en línea:https://rsdjournal.org/index.php/rsd/article/view/45079
Access Level:acceso abierto
Palabra clave:Epilepsia Rolándica
Epilepsia infantil
Neurodesarrollo infantil
Crisis convulsivas
Electroencefalograma
Antiepilépticos
Pediatría.
Epilepsia Rolândica
Neurodesenvolvimento infantil
Crises convulsivas
Eletroencefalograma
Pediatria.
Rolandic Epilepsy
Childhood epilepsy
Child neurodevelopment
Convulsive crises
Electroencephalogram
Antiepileptics
Pediatrics.
Descripción
Sumario:Epilepsy is a medical condition in which there is disturbance of brain activity, characterized by focal, unprovoked or reflex seizures. The objective was to discuss the diagnosis and evolution of Rolandic Epilepsy in childhood, syndromic characteristics and pharmacological therapeutic options. Material and method: integrative literature review using the SCIELO, PUBMED and UPTODATE databases, between 2012 and 2022. 69 articles were identified, being 22 used in the preparation of the work. The results show that Rolandic Epilepsy is the most common neurological disorder in childhood, among other epileptic syndromes, males are the most prevalent and the first manifestation usually occurs before puberty, between seven and nine years of age. The evolution of the clinical history helps in early diagnosis, which represents the best strategy to indicate the correct treatment and avoid future complications of childhood neurodevelopment. For this, the specific test is the electroencephalogram, the result of which reveals obvious abnormalities such as sharp centrotemporal waves and abnormal morphological findings. The prognosis for Rolandic Epilepsy is favorable, due to the self-limited nature of the disease; in most cases, seizures remit before adulthood without causing major damage to the child's neurological development.