22q13 deletion syndrome: communication disorder or autism? Evidence from a specific clinical and neurophysiological phenotype

Phelan–McDermid syndrome is related to terminal 22q13 deletions of various sizes affecting the SHANK3 gene. In this neurodevelopmental disorder, behavioural symptoms of autism spectrum disorder (ASD) are reported in half of cases. Extensive clinical and neurophysiological characterization is lacking...

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Detalles Bibliográficos
Autores principales: Ponson, Laura, Gomot, Marie, Blanc, Romuald, Barthelemy, Catherine, Roux, Sylvie, Munnich, Arnold, Romana, Serge, Aguillon-Hernandez, Nadia, Malan, Valérie, Bonnet-Brilhault, Frédérique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082846/
https://www.ncbi.nlm.nih.gov/pubmed/30089781
http://dx.doi.org/10.1038/s41398-018-0212-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082846/
https://www.ncbi.nlm.nih.gov/pubmed/30089781
http://dx.doi.org/10.1038/s41398-018-0212-9

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