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

Internet

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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