Early Intervention Combined with Targeted Treatment Promotes Cognitive and Behavioral Improvements in Young Children with Fragile X Syndrome

Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability due to an expansion in the full mutation range (>200 CGG repeats) of the promoter region of the FMR1 gene leading to gene silencing. Lack of FMRP, a critical protein for dendritic spine formation and maturation...

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Detalles Bibliográficos
Autores principales: Winarni, Tri Indah, Schneider, Andrea, Borodyanskara, Mariya, Hagerman, Randi J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447258/
https://www.ncbi.nlm.nih.gov/pubmed/23074686
http://dx.doi.org/10.1155/2012/280813

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447258/
https://www.ncbi.nlm.nih.gov/pubmed/23074686
http://dx.doi.org/10.1155/2012/280813

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