Dravet Syndrome in Lebanon: First Report on Cases with SCN1A Mutations

Dravet syndrome, also known as severe myoclonic epilepsy in infancy, is a rare disease characterized by the appearance of different types of seizures in a healthy baby, triggered by various factors and stressful events. We report 8 Lebanese cases referred for molecular analysis of the SCN1A gene. Re...

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Detalhes bibliográficos
Publicado no:Case Rep Med
Main Authors: Alame, Saada, El-Houwayek, Eliane, Nava, Caroline, Sabbagh, Sandra, Fawaz, Ali, Gillart, Anne-Celine, Hasbini, Dana, Depienne, Christel, Mégarbané, André
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2019
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6360541/
https://ncbi.nlm.nih.gov/pubmed/30805006
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/5270503
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