Abstract Caregivers reported on sleep in a convenience sample of 90 children with fragile X syndrome utilizing a standardized assessment tool, the Children's Sleep Habits Questionnaire (CSHQ), and a 14-day sleep diary. CSHQ data indicated that 47% of participants had sleep problems at a level that suggested referral and further evaluation. Sleep diary data indicated high rates of several sleep problems. These problems did not appear to follow a typical developmental trajectory and were not related to gender or demographic variables. Nineteen percent of the sample was currently receiving medication to improve sleep; however, there were no significant differences between those receiving medications and those not receiving medications.
Guadalupe C. Patriarca, Emily J. Ricketts, Melissa Milbert, Laura Trubnick, Erika E. Forbes, Jennifer S. Silk, Cecile D. Ladouceur, Greg J. Siegle, Neal D. Ryan, Allison G Harvey, Ronald E Dahl, Dana L. McMakin
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