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Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling.

Publication ,  Journal Article
Shashi, V; Keshavan, M; Kaczorowski, J; Schoch, K; Lewandowski, KE; McConkie-Rosell, A; Hooper, SR; Kwapil, TR
Published in: J Genet Couns
October 2010

The purpose of this study is to examine the association between parental socio-economic status (SES) and childhood neurocognition and behavior in children with chromosome 22q11.2 deletion syndrome (22q11DS). Although undoubtedly, the deletion of genes in the 22q11.2 interval is primarily responsible for the psychological manifestations, little is known about the role of the environment in either mitigating or contributing to these problems. We examined the association of parental socio-economic status (SES) with cognition and behavior in children with 22q11DS (n = 65) and matched healthy control subjects (n = 52), since SES is a component of family resources. We found that in children with 22q11DS, higher SES correlated with better overall functioning (p < .01) and social skills (p < .01), and less frequent oppositional defiant behavior (p < .001). These findings were in contrast to the control subjects in whom SES correlated with cognition and achievement, but not behavior. Our results indicate that environmental factors influence the behavioral phenotype in children with 22q11DS, providing a framework for developing appropriate interventions. As such, genetic counseling for families with 22q11DS may include consideration of family resources and inclusion of other health professionals, such as social workers, to explore with the family available social supports and resources.

Duke Scholars

Published In

J Genet Couns

DOI

EISSN

1573-3599

Publication Date

October 2010

Volume

19

Issue

5

Start / End Page

535 / 544

Location

United States

Related Subject Headings

  • Social Class
  • Humans
  • Genetics & Heredity
  • Genetic Counseling
  • Cognition Disorders
  • Chromosomes, Human, Pair 22
  • Chromosome Deletion
  • Child Behavior Disorders
  • Child
  • Case-Control Studies
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Shashi, V., Keshavan, M., Kaczorowski, J., Schoch, K., Lewandowski, K. E., McConkie-Rosell, A., … Kwapil, T. R. (2010). Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling. J Genet Couns, 19(5), 535–544. https://doi.org/10.1007/s10897-010-9309-x
Shashi, Vandana, Matcheri Keshavan, Jessica Kaczorowski, Kelly Schoch, Kathryn E. Lewandowski, Allyn McConkie-Rosell, Stephen R. Hooper, and Thomas R. Kwapil. “Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling.J Genet Couns 19, no. 5 (October 2010): 535–44. https://doi.org/10.1007/s10897-010-9309-x.
Shashi V, Keshavan M, Kaczorowski J, Schoch K, Lewandowski KE, McConkie-Rosell A, et al. Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling. J Genet Couns. 2010 Oct;19(5):535–44.
Shashi, Vandana, et al. “Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling.J Genet Couns, vol. 19, no. 5, Oct. 2010, pp. 535–44. Pubmed, doi:10.1007/s10897-010-9309-x.
Shashi V, Keshavan M, Kaczorowski J, Schoch K, Lewandowski KE, McConkie-Rosell A, Hooper SR, Kwapil TR. Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling. J Genet Couns. 2010 Oct;19(5):535–544.
Journal cover image

Published In

J Genet Couns

DOI

EISSN

1573-3599

Publication Date

October 2010

Volume

19

Issue

5

Start / End Page

535 / 544

Location

United States

Related Subject Headings

  • Social Class
  • Humans
  • Genetics & Heredity
  • Genetic Counseling
  • Cognition Disorders
  • Chromosomes, Human, Pair 22
  • Chromosome Deletion
  • Child Behavior Disorders
  • Child
  • Case-Control Studies