Publication:
Congenital Anomalies at Birth: A Hospital Based Study in UAE

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorAryasinghe, L
dc.contributor.authorMoezzi, D
dc.contributor.authorAnsari, TA
dc.contributor.authorMathew, E
dc.contributor.authorSharbatti, SA
dc.contributor.authorShaikh, RB
dc.date.accessioned2026-05-27T04:21:58Z
dc.date.available2026-05-27T04:21:58Z
dc.date.issued2012
dc.descriptionL Aryasinghe Department of Community Medicine, College of Medicine, Gulf Medical University, Ajman D Moezzi Department of Community Medicine, College of Medicine, Gulf Medical University, Ajman TA Ansari Department of Community Medicine, College of Medicine, Gulf Medical University, Ajman E Mathew Department of Community Medicine, College of Medicine, Gulf Medical University, Ajman SA Sharbatti Department of Community Medicine, College of Medicine, Gulf Medical University, Ajman RB Shaikh Department of Community Medicine, College of Medicine, Gulf Medical University, Ajman
dc.description.abstractAbstract: Introduction: It is widely acknowledged that congenital anomalies heavily contribute to infant morbidity and mortality worldwide, with an estimated 9 million infants (7% of all births) born annually having a serious congenital anomaly that result in death or lifelong disability. The objective of our study was to estimate the frequency of congenital anomalies at the Gulf Medical College Hospital and Research Center, Ajman and to estimate the proportion of births with congenital anomalies per 1,000 live births. Materials and Methods: It was a Hospital-Record based descriptive study of the 1,222 consecutive live births from December 2007 to June 2008. Results: There were 84 cases of congenital anomalies among the 1,222 live births; the rate of anomalous births was 68.7 per 1,000 live births or 6.9%. Anomalies of the genitourinary system (40.5%) were the most common, followed by musculoskeletal (28.6%) and cardiovascular (10.7%). Gastrointestinal, chromosomal and multiple system anomalies accounted for 3.6% each and miscellaneous anomalies were seen in 7.1%. Central Nervous system (2.4%) anomalies were the least. Congenital hydrocele (19.0%) was seen to have the highest frequency amongst all recorded anomalies, followed by Talipes or Clubfoot (14.3%). 9.3% of the male and 4.3% of the female population of live births had a congenital anomaly. Birth Weight (p=0.005) and Gender (p=0.001) were found to have significant association with the frequency of birth defects. Maternal Age, gravidity, parity, previous abortions, VDRL and Hepatitis B status, Gestational Diabetes, Pregnancy Induced Hypertension, gestational age, maternal and infant blood group, nationality and consanguinity showed no statistically significant association with congenital anomalies. Conclusion: The proportion of congenital anomalies found in our study is alarmingly high and emphasizes the need for more accessible nationwide screening, counseling and surveillance systems.
dc.identifierhttps://doi.org/10.3126/jnps.v32i2.5995
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6254
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectCongenital anomalies
dc.subjectcongenital malformations
dc.subjectrisk factors
dc.subjectmaternal and infant variables
dc.subjectHospital-record based
dc.titleCongenital Anomalies at Birth: A Hospital Based Study in UAE
dc.typeArticle
dspace.entity.typePublication
local.article.typeOriginal Article
oaire.citation.endPage112
oaire.citation.startPage105
relation.isJournalIssueOfPublicationbee5f04f-02d7-4ebc-9b32-c948670b0393
relation.isJournalIssueOfPublication.latestForDiscoverybee5f04f-02d7-4ebc-9b32-c948670b0393
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
105-112.pdf
Size:
158.82 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.86 KB
Format:
Item-specific license agreed to upon submission
Description:

Collections