Epilepsy and genetic in Rett syndrome: A review

INTRODUCTION: Rett syndrome (RTT) is a severe X‐linked neurodevelopmental disorder that primarily affects girls, with an incidence of 1:10,000–20,000. The diagnosis is based on clinical features: an initial period of apparently normal development (ages 6–12 months) followed by a rapid decline with r...

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Detalles Bibliográficos
Autores principales: Operto, Francesca Felicia, Mazza, Roberta, Pastorino, Grazia Maria Giovanna, Verrotti, Alberto, Coppola, Giangennaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520293/
https://www.ncbi.nlm.nih.gov/pubmed/30929312
http://dx.doi.org/10.1002/brb3.1250

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520293/
https://www.ncbi.nlm.nih.gov/pubmed/30929312
http://dx.doi.org/10.1002/brb3.1250

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