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Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype

Rare neurodevelopmental syndromes often present social cognitive deficits that may underlie difficulties in social interactions and increase the risk of psychosis or autism spectrum disorders. However, little is known regarding the specificities of social cognitive impairment across syndromes while...

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Autores principales: Morel, Aurore, Peyroux, Elodie, Leleu, Arnaud, Favre, Emilie, Franck, Nicolas, Demily, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943552/
https://www.ncbi.nlm.nih.gov/pubmed/29774207
http://dx.doi.org/10.3389/fped.2018.00102
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author Morel, Aurore
Peyroux, Elodie
Leleu, Arnaud
Favre, Emilie
Franck, Nicolas
Demily, Caroline
author_facet Morel, Aurore
Peyroux, Elodie
Leleu, Arnaud
Favre, Emilie
Franck, Nicolas
Demily, Caroline
author_sort Morel, Aurore
collection PubMed
description Rare neurodevelopmental syndromes often present social cognitive deficits that may underlie difficulties in social interactions and increase the risk of psychosis or autism spectrum disorders. However, little is known regarding the specificities of social cognitive impairment across syndromes while it remains a major challenge for the care. Our review provides an overview of social cognitive dysfunctions in rare diseases associated with psychiatric symptoms (with a prevalence estimated between 1 in 1,200 and 1 in 25,000 live births: 22q11.2 deletion syndrome, Angelman syndrome, Fragile X syndrome, Klinefelter syndrome, Prader–Willi syndrome, Rett syndrome, Smith–Magenis syndrome, Turner syndrome, and Williams syndrome) and shed some light on the specific mechanisms that may underlie these skills in each clinical presentation. We first detail the different processes included in the generic expression “social cognition” before summarizing the genotype, psychiatric phenotype, and non-social cognitive profile in each syndrome. Then, we offer a systematic review of the social cognitive abilities and the disturbed mechanisms they are likely associated with. We followed the PRISMA process, including the definition of the relevant search terms, the selection of studies based on clear inclusion, and exclusion criteria and the quality appraisal of papers. We finally provide insights that may have considerable influence on the development of adapted therapeutic interventions such as social cognitive training (SCT) therapies specifically designed to target the psychiatric phenotype. The results of this review suggest that social cognition impairments share some similarities across syndromes. We propose that social cognitive impairments are strongly involved in behavioral symptoms regardless of the overall cognitive level measured by intelligence quotient. Better understanding the mechanisms underlying impaired social cognition may lead to adapt therapeutic interventions. The studies targeting social cognition processes offer new thoughts about the development of specific cognitive training programs, as they highlight the importance of connecting neurocognitive and SCT techniques.
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spelling pubmed-59435522018-05-17 Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype Morel, Aurore Peyroux, Elodie Leleu, Arnaud Favre, Emilie Franck, Nicolas Demily, Caroline Front Pediatr Pediatrics Rare neurodevelopmental syndromes often present social cognitive deficits that may underlie difficulties in social interactions and increase the risk of psychosis or autism spectrum disorders. However, little is known regarding the specificities of social cognitive impairment across syndromes while it remains a major challenge for the care. Our review provides an overview of social cognitive dysfunctions in rare diseases associated with psychiatric symptoms (with a prevalence estimated between 1 in 1,200 and 1 in 25,000 live births: 22q11.2 deletion syndrome, Angelman syndrome, Fragile X syndrome, Klinefelter syndrome, Prader–Willi syndrome, Rett syndrome, Smith–Magenis syndrome, Turner syndrome, and Williams syndrome) and shed some light on the specific mechanisms that may underlie these skills in each clinical presentation. We first detail the different processes included in the generic expression “social cognition” before summarizing the genotype, psychiatric phenotype, and non-social cognitive profile in each syndrome. Then, we offer a systematic review of the social cognitive abilities and the disturbed mechanisms they are likely associated with. We followed the PRISMA process, including the definition of the relevant search terms, the selection of studies based on clear inclusion, and exclusion criteria and the quality appraisal of papers. We finally provide insights that may have considerable influence on the development of adapted therapeutic interventions such as social cognitive training (SCT) therapies specifically designed to target the psychiatric phenotype. The results of this review suggest that social cognition impairments share some similarities across syndromes. We propose that social cognitive impairments are strongly involved in behavioral symptoms regardless of the overall cognitive level measured by intelligence quotient. Better understanding the mechanisms underlying impaired social cognition may lead to adapt therapeutic interventions. The studies targeting social cognition processes offer new thoughts about the development of specific cognitive training programs, as they highlight the importance of connecting neurocognitive and SCT techniques. Frontiers Media S.A. 2018-05-03 /pmc/articles/PMC5943552/ /pubmed/29774207 http://dx.doi.org/10.3389/fped.2018.00102 Text en Copyright © 2018 Morel, Peyroux, Leleu, Favre, Franck and Demily. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Morel, Aurore
Peyroux, Elodie
Leleu, Arnaud
Favre, Emilie
Franck, Nicolas
Demily, Caroline
Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype
title Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype
title_full Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype
title_fullStr Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype
title_full_unstemmed Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype
title_short Overview of Social Cognitive Dysfunctions in Rare Developmental Syndromes With Psychiatric Phenotype
title_sort overview of social cognitive dysfunctions in rare developmental syndromes with psychiatric phenotype
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943552/
https://www.ncbi.nlm.nih.gov/pubmed/29774207
http://dx.doi.org/10.3389/fped.2018.00102
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