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DC Field | Value | Language |
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dc.contributor.author | Ayede, AI | - |
dc.contributor.author | Adeleye, A O | - |
dc.contributor.author | Olusanya, AA | - |
dc.contributor.author | Lawal, T.A | - |
dc.contributor.author | Olusanmi, BA | - |
dc.contributor.author | Ogunkunle, OO | - |
dc.contributor.author | Asinobi, A.O | - |
dc.contributor.author | Adebayo, B.E | - |
dc.contributor.author | Jarrett, OO | - |
dc.contributor.author | Olulana, D.I | - |
dc.contributor.author | Ogudoyin, O.O | - |
dc.contributor.author | Ashubu, O.F | - |
dc.contributor.author | Morhason Bello, I.O | - |
dc.contributor.author | Adekanbi, A.O.A | - |
dc.contributor.author | Baiyeroju, A.M | - |
dc.contributor.author | Joel Medewase, V.I | - |
dc.contributor.author | Ademola, A.D | - |
dc.contributor.author | Olayemi, O | - |
dc.contributor.author | Ogbole, G.I | - |
dc.contributor.author | Akinmoladun, J.A | - |
dc.contributor.author | Agunloye, A.M | - |
dc.contributor.author | Akinrinoye, O.O | - |
dc.contributor.author | Takure, A.O | - |
dc.contributor.author | Oyewole, O.B | - |
dc.contributor.author | Oluwatosin, O.M | - |
dc.contributor.author | Omokhodion, S.I | - |
dc.date.accessioned | 2024-09-17T11:15:22Z | - |
dc.date.available | 2024-09-17T11:15:22Z | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | Afr. J. Med. med. Sci. (2016) 45, 433-438 | en_US |
dc.identifier.issn | 1116-4077 | - |
dc.identifier.uri | http://adhlui.com.ui.edu.ng/jspui/handle/123456789/2907 | - |
dc.description | Article | en_US |
dc.description.abstract | Background: There is a need for a multidisciplinary database that can be used as a potential source for developing a protocol and a guideline for a possible nationwide prospective surveillance of congenital anomalies in Nigeria. Methods: This five-year cross-sectional retrospective survey of data from January 2009 to December 2013 was done at the University College Hospital, Ibadan. Data were collected from the admission records on the wards in 8 specialty units with the most workable documented clinical records of congenital anomalies in their car causing a predesigned proforma. Proportion s of congenital anomalies were determined based on systemic classification of the anomalies and the descriptive terms used were according to the ICD_10-chaptc r XVIII_RCPCH extension. Result: The total number of patients with congenital anomalies whose records were obtained from the ward registers was 1311, there were 75 (5.7%) missing case notes while information was obtained on 1236 (94.3%) patients. There were a total of 1479 anomalies with multiple anomalies seen in 16.1% of the patients. The male/female ratio was 2:1 and multiple births as well as positive family history of birth defects were seen in about 2.4% and 2.2% of cases respectively. Prenatal diagnosis of the anomalies was documented in only 11 cases (0.9%). Only about one in five cases presented within the neonatal period, and defects of the abdominal wall as well as the cranial-facial-orbital regions were the most prevalent. Next were those in t h e cardiovascular, spinal column, anorectal and genital, as well as musculoskeletal systems | en_US |
dc.description.sponsorship | COLLEGE OF MEDICINE, UNIVERSITY OF IBADAN, NIGERIA | en_US |
dc.language.iso | en | en_US |
dc.publisher | COLLEGE OF MEDICINE | en_US |
dc.subject | Congenital | en_US |
dc.subject | Anomaly | en_US |
dc.subject | Ibadan | en_US |
dc.subject | Musculoskeleta | en_US |
dc.title | Congenital anomalies in Ibadan, Nigeria | en_US |
dc.type | Article | en_US |
Appears in Collections: | African Journal of Medicine and Medical Sciences |
Files in This Item:
File | Description | Size | Format | |
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Ayede et al _Congenital_2016.pdf | Article | 12.73 MB | Adobe PDF | View/Open |
Announcements_2016.pdf | Announcement | 376.5 kB | Adobe PDF | View/Open |
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