A Description of Congenital Anomalies Among Infants in Entebbe, Uganda

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dc.contributor.authorNdibazza, Juliet
dc.contributor.authorLule, Swaib
dc.contributor.authorNampijja, Margaret
dc.contributor.authorMpairwe, Harriet
dc.contributor.authorOduru, Gloria
dc.contributor.authorKiggundu, Molly
dc.contributor.authorAkello, Miriam
dc.contributor.authorMuhangi, Lawrence
dc.contributor.authorElliott, Alison M.
dc.date.accessioned2021-12-21T06:09:27Z
dc.date.available2021-12-21T06:09:27Z
dc.date.issued2011
dc.description.abstractData on congenital anomalies from developing countries of the sub-Saharan region are scarce. However, it is important to have comprehensive and reliable data on the description and prevalence of congenital anomalies to allow surveillance and the implementation of appropriate public health strategies for prevention and management. In this study, we describe the profile of congenital anomalies seen in a birth cohort in Entebbe, Uganda. Congenital anomalies were defined as any structural defect present at birth. Pregnant women were recruited to the cohort between 2003 and 2005. Defects present at birth were recorded by the midwife at delivery and by physicians at the routine six-week postnatal visit and at illness-related visits until 1 year of life. The anomalies were classified by organ system according to the 10th version of the World Health Organization International Classification of Diseases (ICD-10). RESULTS: There were 180 infants with a congenital anomaly among 2365 births. The most commonly affected systems were the musculoskeletal (42.7 per 1000 births) and skin (16.1 per 1000 births). The prevalence of major anomalies was 20.3 per 1000 births; 1.7 per 1000 births for cardiac anomalies and 1.3 per 1000 births for neural system anomalies. Forty (22%) of the congenital anomalies were identified at birth, 131 (73%) at the 6- week postnatal visit, and nine (5%) at illness-related visits. Congenital anomalies are common in developing countries. Establishment of comprehensive databases for surveillance would be helpful for surveillance of effects of new exposures, for prevention, management, and health care planning. Birth Defects Research (Part A) 91:857–861, 2011. 2011 Wiley-Liss, Inc.en_US
dc.identifier.citationNdibazza, J., Lule, S., Nampijja, M., Mpairwe, H., Oduru, G., Kiggundu, M., ... & Elliott, A. M. (2011). A description of congenital anomalies among infants in Entebbe, Uganda. Birth Defects Research Part A: , 857-861. DOI: https://doi.org/10.1002/bdra.20838en_US
dc.identifier.urihttps://doi.org/10.1002/bdra.20838
dc.identifier.urihttps://nru.uncst.go.ug/xmlui/handle/123456789/872
dc.language.isoenen_US
dc.publisherClinical and Molecular Teratology,en_US
dc.relation.ispartofseriesClinical and Molecular Teratology;91(9)
dc.subjectCongenital anomaliesen_US
dc.subjectinfantsen_US
dc.subjectepidemiologyen_US
dc.subjectUgandaen_US
dc.subjectAfricaen_US
dc.titleA Description of Congenital Anomalies Among Infants in Entebbe, Ugandaen_US
dc.typeArticleen_US
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