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Delay in skeletal maturity in Malawian children
C P Lewis1, C B D Lavy, W J Harrison
1Department of Orthopaedic Surgery, College of Medicine, University of Malawi, Blantyre.
The Journal of Bone and Joint Surgery. British Volume
|August 22, 2002
Summary
The Greulich and Pyle atlas for skeletal age assessment is inaccurate for Malawian children. Most children showed significantly lower skeletal ages than their chronological ages, indicating the atlas is not globally applicable.
Area of Science:
- Orthopedics
- Pediatrics
- Anthropology
Background:
- The Greulich and Pyle atlas is a standard tool for assessing skeletal maturity and planning orthopedic surgery.
- The atlas was developed using data from institutionalized American children in the 1950s.
- Its applicability to diverse populations, particularly in sub-Saharan Africa, remains unverified.
Purpose of the Study:
- To evaluate the accuracy of the Greulich and Pyle atlas for assessing skeletal age in Malawian children.
- To compare skeletal age with chronological age in a Malawian cohort.
- To investigate potential contributing factors to discrepancies in skeletal age assessment.
Main Methods:
- Skeletal age was assessed using the Greulich and Pyle atlas for 139 Malawian children and young adults.
- Chronological age, height, weight, and body mass index (BMI) were recorded for all participants.
- Statistical analysis, including t-tests, was used to compare skeletal and chronological ages.
Main Results:
- 85.6% of participants (119 out of 139) exhibited a skeletal age lower than their chronological age.
- The mean difference between skeletal and chronological age was 20.0 months, with a maximum difference of 100 months.
- A significant portion of participants (131) had a BMI below the normal range (20-25 kg/m²).
Conclusions:
- The Greulich and Pyle atlas is inaccurate for assessing skeletal age in Malawian children.
- Factors such as poor nutrition and endemic diseases (malaria, diarrhea) are likely contributors to delayed skeletal maturation.
- No correlation was found between reduced BMI and the degree of skeletal age retardation in this cohort.