Intellectual Profiles in KBG-Syndrome: A Wechsler Based Case-Control Study

KBG syndrome is a neurodevelopmental disorder (NDD) caused by loss-of-function of the ANKRD11 gene. The core phenotype comprises developmental delay (DD)/ intellectual disability (ID) and several specific facial dysmorphisms. In addition, both ADHD- and ASD-related symptoms have been mentioned. For...

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Detalles Bibliográficos
Autores principales: van Dongen, Linde C. M., Wingbermühle, Ellen, Oomens, Wouter, Bos-Roubos, Anja G., Ockeloen, Charlotte W., Kleefstra, Tjitske, Egger, Jos I. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742227/
https://www.ncbi.nlm.nih.gov/pubmed/29311865
http://dx.doi.org/10.3389/fnbeh.2017.00248

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742227/
https://www.ncbi.nlm.nih.gov/pubmed/29311865
http://dx.doi.org/10.3389/fnbeh.2017.00248

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