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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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Hoofdauteurs: Sergio Serrada-Tejeda, Patricia Sánchez-Herrera-Baeza, Rosa M. Martínez-Piédrola, Nuria Máximo-Bocanegra, Nuria Trugeda-Pedrajo, M.ª Pilar Rodríguez-Pérez, Gemma Fernández-Gómez, Marta Pérez-de-Heredia-Torres
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: MDPI AG 2023-06-01
Reeks:Children
Onderwerpen:
Phelan–McDermid syndrome
<i>SHANK3</i>
autism spectrum disorder
sensory reactivity
Online toegang:https://www.mdpi.com/2227-9067/10/6/1086
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