Literature DB >> 23742203

Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.

T M Allen1, J Hersh, K Schoch, K Curtiss, S R Hooper, V Shashi.   

Abstract

BACKGROUND: Children with 22q11.2 deletion syndrome (22q11DS) are at risk for social-behavioural and neurocognitive sequelae throughout development. The current study examined the impact of family environmental characteristics on social-behavioural and cognitive outcomes in this paediatric population.
METHOD: Guardians of children with 22q11DS were recruited through two medical genetics clinics. Consenting guardians were asked to complete several questionnaires regarding their child's social, emotional and behavioural functioning, as well as family social environment and parenting styles. Children with 22q11DS were asked to undergo a cognitive assessment, including IQ and achievement testing, and measures of attention, executive function and memory.
RESULTS: Modest associations were found between aspects of the family social environment and parenting styles with social-behavioural and cognitive/academic outcomes. Regression models indicated that physical punishment, socioeconomic status, parental control and family organisation significantly predicted social-behavioural and cognitive outcomes in children with 22q11DS.
CONCLUSION: Characteristics of the family social environment and parenting approaches appear to be associated with functional outcomes of children with 22q11DS. Understanding the impact of environmental variables on developmental outcomes can be useful in determining more effective targets for intervention. This will be important in order to improve the quality of life of individuals affected by 22q11DS.
© 2013 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and John Wiley & Sons Ltd.

Entities:  

Keywords:  DiGeorge syndrome; chromosome 22q11.2 deletion syndrome; family environment; parenting; social-behavioural functioning; velocardiofacial syndrome

Mesh:

Year:  2013        PMID: 23742203      PMCID: PMC4086857          DOI: 10.1111/jir.12054

Source DB:  PubMed          Journal:  J Intellect Disabil Res        ISSN: 0964-2633


  48 in total

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2.  Vulnerability and resilience: a study of high-risk adolescents.

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3.  COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.

Authors:  Vandana Shashi; Timothy D Howard; Matcheri S Keshavan; Jessica Kaczorowski; Margaret N Berry; Kelly Schoch; Edward J Spence; Thomas R Kwapil
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4.  Chronic and discrete stress as predictors of children's adjustment.

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5.  Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome.

Authors:  Kathryn Eve Lewandowski; Vandana Shashi; Peggy M Berry; Thomas R Kwapil
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2007-01-05       Impact factor: 3.568

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Review 7.  Mathematical learning disabilities in children with 22q11.2 deletion syndrome: a review.

Authors:  Bert De Smedt; Ann Swillen; Lieven Verschaffel; Pol Ghesquière
Journal:  Dev Disabil Res Rev       Date:  2009

8.  Affective disorders and other psychiatric diagnoses in children and adolescents with 22q11.2 Deletion Syndrome.

Authors:  Edith M Jolin; Ronald A Weller; Naushad R Jessani; Elaine H Zackai; Donna M McDonald-McGinn; Elizabeth B Weller
Journal:  J Affect Disord       Date:  2009-03-09       Impact factor: 4.839

9.  Parenting, family contexts, and personality characteristics in youngsters with VCFS.

Authors:  P Prinzie; A Swillen; B Maes; P Onghena; A Vogels; A Van Hooste; K Devriendt; C F M Van Lieshout; J P Fryns
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10.  Association of maternal and paternal IQ with offspring conduct, emotional, and attention problem scores. Transgenerational evidence from the 1958 British Birth Cohort Study.

Authors:  Elise Whitley; Catharine R Gale; Ian J Deary; Mika Kivimaki; G David Batty
Journal:  Arch Gen Psychiatry       Date:  2011-10
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  6 in total

Review 1.  Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome.

Authors:  Ania M Fiksinski; Maude Schneider; Clodagh M Murphy; Marco Armando; Stefano Vicari; Jaume M Canyelles; Doron Gothelf; Stephan Eliez; Elemi J Breetvelt; Celso Arango; Jacob A S Vorstman
Journal:  Am J Med Genet A       Date:  2018-09-08       Impact factor: 2.802

2.  Childhood Predictors of Young Adult Social Functioning in 22q11.2 Deletion Syndrome.

Authors:  Kayla E Wagner; Wendy R Kates; Wanda Fremont; Kevin M Antshel
Journal:  J Autism Dev Disord       Date:  2017-08

3.  Parental Expressed Emotion, Parenting Stress, and Behavioral Problems of Young Children with 22q11.2 Deletion Syndrome and Idiopathic Autism Spectrum Disorder.

Authors:  Yaffa Serur; Efrat Sher-Censor; Dafna Sofrin-Frumer; Keren Daon; Dolly Sobol-Havia; Ronnie Weinberger; Cory Shulman; Doron Gothelf
Journal:  Child Psychiatry Hum Dev       Date:  2022-01-27

Review 4.  A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome.

Authors:  Ania M Fiksinski; Gil D Hoftman; Jacob A S Vorstman; Carrie E Bearden
Journal:  Mol Psychiatry       Date:  2022-10-03       Impact factor: 13.437

Review 5.  Deletion Syndrome 22q11.2: A Systematic Review.

Authors:  Jonathan Cortés-Martín; Nuria López Peñuela; Juan Carlos Sánchez-García; Maria Montiel-Troya; Lourdes Díaz-Rodríguez; Raquel Rodríguez-Blanque
Journal:  Children (Basel)       Date:  2022-08-03

6.  Psychological Adjustment of Children and Adolescents with 22q11.2 Deletion Syndrome and Their Mothers' Stress and Coping-A Longitudinal Study.

Authors:  Wolfgang Briegel; Christoph Andritschky
Journal:  Int J Environ Res Public Health       Date:  2021-03-08       Impact factor: 3.390

  6 in total

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