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Global prevalence of Rett syndrome: systematic review and meta-analysis

BACKGROUND: Rett syndrome is a rare, severe neurodevelopmental disorder. Almost all cases occur in girls, in association with spontaneous (non-inherited) mutations involving the methyl-CpG-binding protein 2 gene located on the X chromosome. Diagnostic criteria for typical Rett syndrome require a per...

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Detalles Bibliográficos
Autores principales:	Petriti, Uarda, Dudman, Daniel C., Scosyrev, Emil, Lopez-Leon, Sandra
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2023
Materias:	Systematic Review Update
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841621/ https://www.ncbi.nlm.nih.gov/pubmed/36642718 http://dx.doi.org/10.1186/s13643-023-02169-6

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