Citation

Briegel W, Schneider M, Schwab KO. Child Care Health Dev. 2008; 34(6): 795-800.

Copyright

(Copyright © 2008, John Wiley and Sons)

DOI

10.1111/j.1365-2214.2008.00850.x

PMID

unavailable

Abstract

Background 22q11.2 deletion syndrome can be associated with a variety of somatic symptoms, developmental delays and psychiatric disorders. At present, there is little information on behaviour problems, parental stress and possible relations between these factors. Therefore, this study investigates behaviour problems of children and adolescents with 22q11.2DS, and their primary caregivers’ stress.

Methods Parents of 4–17 year old subjects known to the German 22q11.2 deletion syndrome foundation were anonymously asked to fill out several questionnaires, e.g. the Child Behavior Checklist 4–18 (CBCL/4–18).

Results The primary caregivers of 77/126 children [43 males, 34 females, mean age: 8;0 (4;0–16;11) years] sent back filled‐out questionnaires. Forty‐six of 76 subjects were rated as clinical on at least one of the CBCL‐scales. Males had significantly higher scores on the total problems scale and the internalizing problems scale than females. The patients’ age correlated with several CBCL‐scales. Eleven of 49 subjects were suspicious of an autism spectrum disorder. Compared with the general population, but not with other parents of mentally and/or physically handicapped children, the primary caregivers experienced higher levels of stress, but showed normal life satisfaction.

Conclusions In spite of high rates of clinical behaviour problems among children and adolescents with 22q11.2DS and despite increased parental stress, most primary caregivers seem to have effective coping strategies, e.g. partnership support, to sustain normal levels of life satisfaction.