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Published on: October 2, 2019
Sleep profiles in children with Down syndrome
Julia L Bassell1, Han Phan2, Roberta Leu2
1Department of Human Genetics, Emory University, Atlanta, Georgia.
Insights
Most children with Down syndrome (DS) experience sleep problems, often starting young and persisting with age. Ongoing monitoring is crucial, even after surgery for obstructive sleep apnea (OSA).
Area of Science:
- Genetics
- Pediatrics
- Sleep Medicine
Background:
- Down syndrome (DS), caused by Trisomy 21, is the leading genetic cause of intellectual disability.
- Sleep disturbances and obstructive sleep apnea (OSA) are prevalent in DS but frequently overlooked.
- High prevalence of sleep issues in children with DS necessitates further investigation.
Purpose of the Study:
- To assess sleep behaviors in children with Down syndrome using a standardized questionnaire.
- To determine the prevalence and characteristics of sleep problems in this population.
- To inform clinical practice regarding sleep management in children with DS.
Main Methods:
- Cross-sectional study involving 108 children with DS (ages 1.50–13.40 years).
- Caregiver-reported sleep behaviors were assessed using the Children's Sleep Habit Questionnaire (CSHQ).
- Data analysis focused on identifying patterns and prevalence of sleep issues.
Main Results:
- 76% of children with DS exhibited significant sleep problems.
- Sleep issues were reported to begin at a young age and persist or recur with age.
- Even after adenoidectomy and tonsillectomy for OSA, sleep problems continued in some children.
Conclusions:
- Sleep problems are a common and persistent issue in children with Down syndrome.
- Early recognition and ongoing monitoring of sleep are essential for this population.
- Interventions and anticipatory guidance are needed to manage sleep disturbances in DS.
Abstract:
Down syndrome (DS) is the most common genetic cause of intellectual disability and results from an extra chromosome 21 (Trisomy 21). Sleep issues and/or obstructive sleep apnea (OSA) are assumed to be part of the DS phenotype with a high prevalence but are often under recognized. This cross-sectional study of children with DS examines the caregiver-reported sleep behaviors of 108 children with DS, ranging in age from 1.50 to 13.40 years (mean = 5.18 years) utilizing a standardized assessment tool, the Children's Sleep Habit Questionnaire (CSHQ). The CSHQ revealed 76% of children with DS had sleep problems, which began at a young age, and continue to persist and may recur with increasing age. Furthermore, children with DS who undergone adenoidectomy and tonsillectomy for OSA continued to have sleep problems suggesting that ongoing monitoring of sleep issues is needed in this population. Implications of sleep problems and recommended anticipatory guidance and intervention are discussed.
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