Prospective One-Year Follow-Up of Sensory Processing in Phelan–McDermid Syndrome

Background: Phelan–McDermid syndrome (PMS) is caused by the loss (deletion) of a small portion of chromosome 22 in a region designated q13.3 (22q13.3 deletion). PMS is one of the most common genetic forms of autism spectrum disorder (ASD) in which sensory reactivity difficulties have been described...

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Detalles Bibliográficos
Autores principales: Serrada-Tejeda, Sergio, Sánchez-Herrera-Baeza, Patricia, Martínez-Piédrola, Rosa M., Máximo-Bocanegra, Nuria, Trugeda-Pedrajo, Nuria, Rodríguez-Pérez, M.ª Pilar, Fernández-Gómez, Gemma, Pérez-de-Heredia-Torres, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296885/
https://www.ncbi.nlm.nih.gov/pubmed/37371317
http://dx.doi.org/10.3390/children10061086

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296885/
https://www.ncbi.nlm.nih.gov/pubmed/37371317
http://dx.doi.org/10.3390/children10061086

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