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The pattern of Down syndrome among children in Qatar: a population-based study
Atqah Abdul Wahab1, Abdulbari Bener, Amy L Sandridge
1Department of Pediatrics, Hamad Medical Corporation , Hamad General Hospital, Doha, Qatar.
Insights
Down Syndrome (DS) affects 19.5 per 10,000 live births in Qatar children under five. Regular trisomy is the most common abnormality, with congenital heart problems affecting half of affected children.
Area of Science:
- Genetics
- Pediatrics
- Public Health
Background:
- Retrospective descriptive study on Down Syndrome (DS) prevalence in children under five in Qatar.
- Data collected from Hamad Medical Corporation hospitals over a six-year period (2000-2005).
- 146 children diagnosed with DS during the study period.
Purpose of the Study:
- Determine the prevalence pattern of Down Syndrome (DS) in children under five years of age in Qatar.
- Analyze sociodemographic characteristics, genetic, and family history of DS cases.
- Investigate the relationship between DS and maternal age.
Main Methods:
- Diagnostic classification based on International Classification of Disease 10th Revision (ICD-10).
- Review of medical records including sociodemographic data, genetic and family history, pedigree analysis, and clinical genetic examination.
- Prevalence calculation per 10,000 live births.
Main Results:
- Overall DS prevalence of 19.5 per 10,000 live births.
- DS was more common in non-Qataris (59.6%) than Qataris (40.4%).
- Higher frequency in infants under one year (40.4%), with regular trisomy (98%) and congenital heart problems (51.7%) being common.
Conclusions:
- Identification of specific chromosomal abnormalities in DS is crucial for accurate genetic counseling.
- Understanding recurrence risks and available options for parents is vital.
- Significant relationship observed between DS and maternal age.
Background:
The objective of the present study was to determine the prevalence pattern of Down Syndrome (DS) in children <5 years of age in the State of Qatar. This is a retrospective descriptive study. The study was conducted in the Hamad General Hospital, Women's Hospital, and Rumailah Hospital (Hamad Medical Corporation). A total of 146 children were reported as having DS during the 6-year period from 1 January 2000 to December 31, 2005.
Methods:
The diagnostic classification of definitive DS was made in accordance with criteria based on the International Classification of Disease 10th Revision (ICD-10). The data collected from the medical records included sociodemographic characteristics of the children, genetic and family history, pedigree analysis, and clinical genetic examination.
Results:
A total of 146 children were diagnosed with DS during the last 6-year period and the prevalence rate is 19.5 per 10,000 live births. Of these, 40.4% were Qataris and 59.6% were non-Qataris. DS was slightly more common in boys (52.7%) than girls (47.3%). Infants <1 year old had the highest frequency of DS (40.4%), followed by children (1-2) years (26%). The most common abnormality was regular trisomy (98%). Also, one-half of the studied children had congenital heart problems (51.7%). There is a significant relationship between DS and maternal age as reported by other studies in other countries.
Conclusion:
The identification of specific types of chromosomal abnormalities in DS children is important as it enables clinicians to accurately counsel the parent regarding the recurrence risk and available options.
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