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Epidemiological and clinical profile of congenital malformations in Benghazi Pediatric Hospital

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dc.contributor.author Alkarshouf, Yasmeenah S. H
dc.contributor.author Greiw, Azza E. H
dc.contributor.author El Misallati, Abd Alsalam
dc.date.accessioned 2020-10-06T14:35:08Z
dc.date.available 2020-10-06T14:35:08Z
dc.date.issued 2019-12-31
dc.identifier.issn 2663-1407
dc.identifier.uri http://repository.uob.edu.ly/handle/123456789/1306
dc.description.abstract Objectives: The objectives were to assess the nature and the frequency of congenital malformations among infants and children who were admitted to Benghazi pediatric hospital and to study the associated maternal and neonatal risk factors. Patients and methods: A cross-sectional study design was used for this study. It included infants and children aged (0-16 yrs.) who were admitted to Benghazi Children Hospital and who were following the genetic clinic, during the period of March 2016 to March 2017. These cases had dysmorphic features and multiple congenital malformations. A record sheet was used to collect the required data from cases. Results: The total number of patients was 81 children, 51.85% were females, 48.15% were males and infants represented 62%. Cases with a history of consanguineous marriage represented 28.40%. Equal proportions of mothers (1.23%) had a history of diabetes, epilepsy and cardiomyopathy. Nearly a quarter of cases, (24.69%) were low birth weight. Prevalence of congenital malformations (CMs) according to organs were; CVS (50.62%), musculoskeletal (44.44%), eye (24.7%), limb defect (17.3%), GIT (14.8%), ear (14.8%), CNS (11.11%), urogenital (external & internal)(11%), cleft lip & palate (9.9%) and Trisomy 21 syndrome (48.1%). Trisomy 21 syndrome have a high frequency of CHD compared to other syndromes; 67.9% had CHD, P=.01. Most cases (90%) died within the first year of life, p=.002. Twenty-six percent of the studied population died during the study period. Conclusion: Most children with CMs and chromosomal abnormalities died within the first year of life. There is a limitation of screening tools, which could lead to imprecise genetic counseling. CM is a significant cause of morbidity and admission. The highest prevalence of CMs was CVS. Trisomy 21 syndrome was the most prevalent chromosomal abnormalities; these cases were at more risk to have CHD compared to other syndromes. There is a shortage of medical services, which applied as segmental services. en_US
dc.language.iso en en_US
dc.publisher Universty of Benghazi en_US
dc.relation.ispartofseries Volume 10, Number 1;1
dc.subject Congenital malformations (CMs) en_US
dc.subject Trisomy 21 en_US
dc.subject Congenital heart disease en_US
dc.title Epidemiological and clinical profile of congenital malformations in Benghazi Pediatric Hospital en_US
dc.type Working Paper en_US


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