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dc.contributor.authorSANDRIDGE, Amy L.
dc.contributor.authorBener, Abdulbari
dc.contributor.authorHOFFMANN, Georg F.
dc.contributor.authorWAHAB, Atqah Abdul
dc.date.accessioned2021-03-05T20:23:30Z
dc.date.available2021-03-05T20:23:30Z
dc.date.issued2006
dc.identifier.citationWAHAB A. A. , Bener A., SANDRIDGE A. L. , HOFFMANN G. F. , "The pattern of Down syndrome among children in Qatar: A population-based study", BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, cilt.76, ss.609-612, 2006
dc.identifier.issn1542-0752
dc.identifier.othervv_1032021
dc.identifier.otherav_d3f376c4-884f-4850-9303-066244d9ed1c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/139895
dc.identifier.urihttps://doi.org/10.1002/bdra.20290
dc.description.abstractBACKGROUND:,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.
dc.language.isoeng
dc.subjectFarmasötik Toksikoloji
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectMikrobiyal Genetik
dc.subjectTemel Bilimler
dc.subjectEczacılık
dc.subjectMeslek Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectTOKSİKOLOJİ
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGELİŞİMSEL BİYOLOJİ
dc.titleThe pattern of Down syndrome among children in Qatar: A population-based study
dc.typeMakale
dc.relation.journalBIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
dc.contributor.department, ,
dc.identifier.volume76
dc.identifier.issue8
dc.identifier.startpage609
dc.identifier.endpage612
dc.contributor.firstauthorID95949


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