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 re...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Brain and behavior 2019-05, Vol.9 (5), p.e01250-n/a
Hauptverfasser:	Operto, Francesca Felicia, Mazza, Roberta, Pastorino, Grazia Maria Giovanna, Verrotti, Alberto, Coppola, Giangennaro
Format:	Artikel
Sprache:	eng
Schlagworte:	Congenital diseases Convulsions & seizures Epilepsy Epilepsy - genetics Eye contact Forkhead Transcription Factors - genetics Gait Genes genetic Genetic Association Studies Genetic counseling Genetic Predisposition to Disease Genotype & phenotype Humans Intellectual disabilities Methyl-CpG-Binding Protein 2 - genetics Microcephaly Motor ability Mutation Nerve Tissue Proteins - genetics Neurodevelopmental disorders Original Research Protein-Serine-Threonine Kinases - genetics Rett syndrome Rett Syndrome - genetics Rett Syndrome - physiopathology Scoliosis Severity of Illness Index Social interaction Stereotypes
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!