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Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome

BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is a common neurogenetic syndrome associated with high rates of psychosis. The aims of the present study were to identify the unique temperament traits that characterize children with 22q11.2DS compared to children with Williams syndrome (WS) and typ...

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Autores principales: Schonherz, Yael, Davidov, Maayan, Knafo, Ariel, Zilkha, Hadas, Shoval, Gal, Zalsman, Gil, Frisch, Amos, Weizman, Abraham, Gothelf, Doron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923103/
https://www.ncbi.nlm.nih.gov/pubmed/24517288
http://dx.doi.org/10.1186/1866-1955-6-3
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author Schonherz, Yael
Davidov, Maayan
Knafo, Ariel
Zilkha, Hadas
Shoval, Gal
Zalsman, Gil
Frisch, Amos
Weizman, Abraham
Gothelf, Doron
author_facet Schonherz, Yael
Davidov, Maayan
Knafo, Ariel
Zilkha, Hadas
Shoval, Gal
Zalsman, Gil
Frisch, Amos
Weizman, Abraham
Gothelf, Doron
author_sort Schonherz, Yael
collection PubMed
description BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is a common neurogenetic syndrome associated with high rates of psychosis. The aims of the present study were to identify the unique temperament traits that characterize children with 22q11.2DS compared to children with Williams syndrome (WS) and typically developing (TD) controls, and to examine temperamental predictors of the emergence of psychosis in 22q11.2DS. METHODS: The temperament of 55 children with 22q11.2DS, 36 with WS, and 280 TD children was assessed using the Emotionality, Activity, Sociability (EAS) Temperament Survey, Parental Ratings. The presence of a psychotic disorder was evaluated in 49 children and adolescents with 22q11.2DS at baseline and again 5.43 ± 2.23 years after baseline temperament assessment. RESULTS: Children with 22q11.2DS scored higher on Shyness compared to WS and TD controls. Children with 22q11.2DS and WS scored higher on Emotionality and lower on Activity compared to TD controls. Shyness was more severe in older compared to younger children with 22q11.2DS. Baseline Shyness scores significantly predicted the later emergence of a psychotic disorder at follow-up, in children with 22q11.2DS. CONCLUSIONS: Our results suggest that shyness is an early marker associated with the later emergence of psychosis in 22q11.2DS.
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spelling pubmed-39231032014-02-14 Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome Schonherz, Yael Davidov, Maayan Knafo, Ariel Zilkha, Hadas Shoval, Gal Zalsman, Gil Frisch, Amos Weizman, Abraham Gothelf, Doron J Neurodev Disord Research BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is a common neurogenetic syndrome associated with high rates of psychosis. The aims of the present study were to identify the unique temperament traits that characterize children with 22q11.2DS compared to children with Williams syndrome (WS) and typically developing (TD) controls, and to examine temperamental predictors of the emergence of psychosis in 22q11.2DS. METHODS: The temperament of 55 children with 22q11.2DS, 36 with WS, and 280 TD children was assessed using the Emotionality, Activity, Sociability (EAS) Temperament Survey, Parental Ratings. The presence of a psychotic disorder was evaluated in 49 children and adolescents with 22q11.2DS at baseline and again 5.43 ± 2.23 years after baseline temperament assessment. RESULTS: Children with 22q11.2DS scored higher on Shyness compared to WS and TD controls. Children with 22q11.2DS and WS scored higher on Emotionality and lower on Activity compared to TD controls. Shyness was more severe in older compared to younger children with 22q11.2DS. Baseline Shyness scores significantly predicted the later emergence of a psychotic disorder at follow-up, in children with 22q11.2DS. CONCLUSIONS: Our results suggest that shyness is an early marker associated with the later emergence of psychosis in 22q11.2DS. BioMed Central 2014 2014-02-11 /pmc/articles/PMC3923103/ /pubmed/24517288 http://dx.doi.org/10.1186/1866-1955-6-3 Text en Copyright © 2014 Schonherz et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research
Schonherz, Yael
Davidov, Maayan
Knafo, Ariel
Zilkha, Hadas
Shoval, Gal
Zalsman, Gil
Frisch, Amos
Weizman, Abraham
Gothelf, Doron
Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
title Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
title_full Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
title_fullStr Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
title_full_unstemmed Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
title_short Shyness discriminates between children with 22q11.2 deletion syndrome and Williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
title_sort shyness discriminates between children with 22q11.2 deletion syndrome and williams syndrome and predicts emergence of psychosis in 22q11.2 deletion syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923103/
https://www.ncbi.nlm.nih.gov/pubmed/24517288
http://dx.doi.org/10.1186/1866-1955-6-3
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