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The Broader Autism Phenotype and Its Implications on the Etiology and Treatment of Autism Spectrum Disorders

The presence of autism-related traits has been well documented in undiagnosed family members of individuals with autism spectrum disorder (ASD). The most common finding is mild impairments in social and communication skills that are similar to those shown by individuals with autism, but exhibited to...

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Detalles Bibliográficos
Autores principales: Gerdts, Jennifer, Bernier, Raphael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420416/
https://www.ncbi.nlm.nih.gov/pubmed/22937250
http://dx.doi.org/10.1155/2011/545901
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author Gerdts, Jennifer
Bernier, Raphael
author_facet Gerdts, Jennifer
Bernier, Raphael
author_sort Gerdts, Jennifer
collection PubMed
description The presence of autism-related traits has been well documented in undiagnosed family members of individuals with autism spectrum disorder (ASD). The most common finding is mild impairments in social and communication skills that are similar to those shown by individuals with autism, but exhibited to a lesser degree. Termed the broader autism phenotype (BAP), these traits suggest a genetic liability for autism-related traits in families. Genetic influence in autism is strong, with identical twins showing high concordance for the diagnosis and related traits and approximately 20% of all ASD cases having an identified genetic mechanism. This paper highlights the studies conducted to date regarding the BAP and considers the implications of these findings for the etiology and treatment of ASD.
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spelling pubmed-34204162012-08-30 The Broader Autism Phenotype and Its Implications on the Etiology and Treatment of Autism Spectrum Disorders Gerdts, Jennifer Bernier, Raphael Autism Res Treat Review Article The presence of autism-related traits has been well documented in undiagnosed family members of individuals with autism spectrum disorder (ASD). The most common finding is mild impairments in social and communication skills that are similar to those shown by individuals with autism, but exhibited to a lesser degree. Termed the broader autism phenotype (BAP), these traits suggest a genetic liability for autism-related traits in families. Genetic influence in autism is strong, with identical twins showing high concordance for the diagnosis and related traits and approximately 20% of all ASD cases having an identified genetic mechanism. This paper highlights the studies conducted to date regarding the BAP and considers the implications of these findings for the etiology and treatment of ASD. Hindawi Publishing Corporation 2011 2011-08-17 /pmc/articles/PMC3420416/ /pubmed/22937250 http://dx.doi.org/10.1155/2011/545901 Text en Copyright © 2011 J. Gerdts and R. Bernier. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Gerdts, Jennifer
Bernier, Raphael
The Broader Autism Phenotype and Its Implications on the Etiology and Treatment of Autism Spectrum Disorders
title The Broader Autism Phenotype and Its Implications on the Etiology and Treatment of Autism Spectrum Disorders
title_full The Broader Autism Phenotype and Its Implications on the Etiology and Treatment of Autism Spectrum Disorders
title_fullStr The Broader Autism Phenotype and Its Implications on the Etiology and Treatment of Autism Spectrum Disorders
title_full_unstemmed The Broader Autism Phenotype and Its Implications on the Etiology and Treatment of Autism Spectrum Disorders
title_short The Broader Autism Phenotype and Its Implications on the Etiology and Treatment of Autism Spectrum Disorders
title_sort broader autism phenotype and its implications on the etiology and treatment of autism spectrum disorders
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420416/
https://www.ncbi.nlm.nih.gov/pubmed/22937250
http://dx.doi.org/10.1155/2011/545901
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