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Updated: Jul 31, 2025

Assessment of Child Anthropometry in a Large Epidemiologic Study
Published on: February 2, 2017
Severe obesity and global developmental delay in preschool children: Findings from a Canadian Paediatric Surveillance
Nicole D Gehring1, Catherine S Birken2, Stacey Belanger3
1School of Public Health, University of Alberta, Edmonton, Alberta, Canada.
Insights
Severe obesity and global developmental delay co-occur in Canadian preschoolers, with a minimum incidence of 3.3 per 100,000. Early identification and genetic testing are crucial for managing these complex cases.
Area of Science:
- Pediatric Health
- Developmental Pediatrics
- Obesity Research
Background:
- The co-occurrence of severe obesity (SO) and global developmental delay (GDD) in Canadian preschool children is not well-documented.
- SO and GDD may necessitate specific syndromic diagnoses and tailored management strategies.
Purpose of the Study:
- To determine the minimum incidence of co-occurring SO and GDD in Canadian children aged 5 years and under.
- To identify the age of onset and risk factors associated with this dual diagnosis.
- To examine health care utilization patterns for children with co-presenting SO and GDD.
Main Methods:
- Utilized the Canadian Paediatric Surveillance Program (CPSP) with monthly reporting forms from February 2018 to January 2020.
- Included children aged 5 years and under with new diagnoses of SO and GDD.
- Employed descriptive statistics and qualitative content analysis for collected data.
Main Results:
- Forty-seven cases were identified (64% male; mean age 3.5 years), with minimum incidence at 3.3 cases per 100,000 annually.
- Common co-occurring issues included behavioral problems, snoring, and asthma; maternal obesity and neonatal intensive care were noted risk factors.
- Genetic testing (microarray) was performed on 57% of children, and diverse clinical services were accessed, though family and service access challenges were reported.
Conclusions:
- Children with co-occurring SO and GDD present with multiple comorbidities requiring prompt identification and specialized care.
- Early referral to appropriate services and consideration of genetic testing for obesity syndromes are recommended.
- Addressing barriers to care for families is essential for effective management.
Background:
The co-presentation of severe obesity (SO) and global developmental delay (GDD) in Canadian preschool children has not been examined. However, SO and GDD may require syndromic diagnoses and unique management considerations.
Objectives:
To determine (1) minimum incidence; (2) age of onset and risk factors; and (3) health care utilization for co-presenting SO and GDD.
Methods:
Through the Canadian Paediatric Surveillance Program (CPSP), a monthly form was distributed to participants from February 2018 to January 2020 asking for reports of new cases of SO and GDD among children ≤5 years of age. We performed descriptive statistics for quantitative questions and qualitative content analysis for open-ended questions.
Results:
Forty-seven cases (64% male; 51% white; mean age: 3.5 ± 1.2 years) were included. Age of first weight concern was 2.5 ± 1.3 years and age of GDD diagnosis was 2.7 ± 1.4 years. Minimum incidence of SO and GDD was 3.3 cases per 100,000 for ≤5 years of age per year. Identified problems included school and/or behavioural problems (n = 17; 36%), snoring (n = 14; 30%), and asthma/recurrent wheeze (n = 10; 21%). Mothers of 32% of cases (n = 15) had obesity and 21% of cases (n = 10) received neonatal intensive care. Microarray was ordered for 57% (n = 27) of children. A variety of clinicians and services were accessed. As reported by CPSP participants, challenges faced by families and health service access were barriers to care.
Conclusion:
Children with SO and GDD have multiple comorbidities, and require early identification and referral to appropriate services. These cases may also benefit from additional testing to rule out known genetic obesity syndromes.
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