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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Bibliografiske detaljer
Udgivet i:Brain Behav
Main Authors: Operto, Francesca Felicia, Mazza, Roberta, Pastorino, Grazia Maria Giovanna, Verrotti, Alberto, Coppola, Giangennaro
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2019
Fag:
Original Research
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6520293/
https://ncbi.nlm.nih.gov/pubmed/30929312
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/brb3.1250
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