The pattern of Down syndrome among children in Qatar: A population-based study

被引:13
作者
Wahab, Atqah Abdul
Bener, Abdulbari
Sandridge, Amy L.
Hoffmann, Georg F.
机构
[1] Hamad Gen Hosp, Hamad Med Corp, Weill Cornell Med Coll Qatar, Dept Med Stat & Epidemiol, Doha, Qatar
[2] Hamad Gen Hosp, Hamad Med Corp, Dept Pediat, Doha, Qatar
[3] Univ Manchester, Sch Epidemiol & Hlth Sci, Populat Hlth Unit, Dept Evidence, Manchester M13 9PL, Lancs, England
[4] Weill Cornell Med Coll, Dept Publ Hlth, Doha, Qatar
[5] Heidelberg Univ, Dept Pediat, Heidelberg, Germany
关键词
epidemiology; Down syndrome; prevalence; maternal age; Qatar;
D O I
10.1002/bdra.20290
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 I 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 high. est 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.
引用
收藏
页码:609 / 612
页数:4
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