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

Publication ,  Journal Article
Allen, TM; Hersh, J; Schoch, K; Curtiss, K; Hooper, SR; Shashi, V
Published in: J Intellect Disabil Res
January 2014

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.

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Published In

J Intellect Disabil Res

DOI

EISSN

1365-2788

Publication Date

January 2014

Volume

58

Issue

1

Start / End Page

31 / 47

Location

England

Related Subject Headings

  • Social Behavior
  • Rehabilitation
  • Regression Analysis
  • Predictive Value of Tests
  • Parents
  • Parenting
  • Male
  • Intellectual Disability
  • Humans
  • Female
 

Citation

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Allen, T. M., Hersh, J., Schoch, K., Curtiss, K., Hooper, S. R., & Shashi, V. (2014). Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome. J Intellect Disabil Res, 58(1), 31–47. https://doi.org/10.1111/jir.12054
Allen, T. M., J. Hersh, K. Schoch, K. Curtiss, S. R. Hooper, and V. Shashi. “Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.J Intellect Disabil Res 58, no. 1 (January 2014): 31–47. https://doi.org/10.1111/jir.12054.
Allen TM, Hersh J, Schoch K, Curtiss K, Hooper SR, Shashi V. Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome. J Intellect Disabil Res. 2014 Jan;58(1):31–47.
Allen, T. M., et al. “Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.J Intellect Disabil Res, vol. 58, no. 1, Jan. 2014, pp. 31–47. Pubmed, doi:10.1111/jir.12054.
Allen TM, Hersh J, Schoch K, Curtiss K, Hooper SR, Shashi V. Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome. J Intellect Disabil Res. 2014 Jan;58(1):31–47.
Journal cover image

Published In

J Intellect Disabil Res

DOI

EISSN

1365-2788

Publication Date

January 2014

Volume

58

Issue

1

Start / End Page

31 / 47

Location

England

Related Subject Headings

  • Social Behavior
  • Rehabilitation
  • Regression Analysis
  • Predictive Value of Tests
  • Parents
  • Parenting
  • Male
  • Intellectual Disability
  • Humans
  • Female