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dc.contributor.authorDastgiri, S
dc.contributor.authorImani, S
dc.contributor.authorKalankesh, L
dc.contributor.authorBarzegar, M
dc.contributor.authorHeidarzadeh, M
dc.date.accessioned2018-08-26T06:33:46Z
dc.date.available2018-08-26T06:33:46Z
dc.date.issued2007
dc.identifier10.1111/j.1365-2214.2006.00720.x
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/43829
dc.description.abstractAt least one congenital anomaly is present in between 1% and 6% of all infants throughout the world. The aim of this study was to document some epidemiological features of congenital anomalies in the North-West of Iran.The study cases (n = 1574) comprised all births registered/notified to three university-hospitals of Tabriz University of Medical Sciences, Iran, from 2000 to 2004.Total prevalence of congenital anomalies was 165.5 per 10 000 births [95% confidence interval (CI): 157-174]. Genito-urinary tract and kidney defects, anomalies of nervous system and limb anomalies accounted proportionally for more than 65% of anomalies in the region. The total prevalence of congenital anomalies in the study area increased from 104.6 per 10 000 births in 2000 (95% CI: 90-119) to 170.1 per 10 000 births in 2004 (95% CI: 152-189).It is concluded that the data from this cross-sectional study of congenital anomalies in the North-West of Iran may be used as the baseline information to establish a population-based registry of birth defects in the area for health care and research purposes.
dc.language.isoEnglish
dc.relation.ispartofChild: care, health and development
dc.subjectCongenital Abnormalities
dc.subjectCross-Sectional Studies
dc.subjectFemale
dc.subjectHumans
dc.subjectInfant, Newborn
dc.subjectIran
dc.subjectLimb Deformities, Congenital
dc.subjectMale
dc.subjectNervous System Malformations
dc.subjectPrevalence
dc.subjectUrogenital Abnormalities
dc.titleCongenital anomalies in Iran: a cross-sectional study on 1574 cases in the North-West of country.
dc.typearticle
dc.citation.volume33
dc.citation.issue3
dc.citation.spage257
dc.citation.epage61
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1111/j.1365-2214.2006.00720.x


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