Prevalence of associated extracardiac anomalies in prenatally diagnosed congenital heart diseases
DC Field | Value | Language |
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dc.contributor.author | Chang, C.-S. | - |
dc.contributor.author | Hong, S.- Y. | - |
dc.contributor.author | Kim, S.-Y. | - |
dc.contributor.author | Kim, Y.-M. | - |
dc.contributor.author | Sung, J.-H. | - |
dc.contributor.author | Choi, S.-J. | - |
dc.contributor.author | Oh, S.-Y. | - |
dc.contributor.author | Roh, C.-R. | - |
dc.contributor.author | Song, J. | - |
dc.contributor.author | Huh, J. | - |
dc.contributor.author | Kang, I.-S. | - |
dc.date.accessioned | 2023-03-08T11:07:29Z | - |
dc.date.available | 2023-03-08T11:07:29Z | - |
dc.date.issued | 2021-03-18 | - |
dc.identifier.issn | 1932-6203 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/62523 | - |
dc.description.abstract | Objective To investigate the prevalence of extracardiac anomalies (ECA) in prenatally diagnosed congenital heart diseases (CHD), and to provide more information for counseling of women with prenatally diagnosed fetal CHD. Methods This was a retrospective cohort study of 791 cases of fetal CHD diagnosed by prenatal ultrasound from January 2005 to April 2018. Associated ECAs included extracardiac structural malformation (ECM), chromosomal anomaly, and 22q11.2 microdeletion. CHD was classified into 10 groups according to a modified anatomic and clinical classification of congenital heart defects. Results The overall prevalence of ECA in our CHD cohort was 28.6% (226/791): ECM, 25.3%; chromosomal anomaly, 11.7%; and 22q11.2 microdeletion, 5.5%. For those with ECM, ventricular septal defect (VSD) had the highest prevalence (34.5%), followed by anomalies of atrioventricular junctions and valves (28.8%) and heterotaxy (26.9%). For those with chromosomal anomaly, anomalies of atrioventricular junctions and valves had the highest prevalence (37.5%), followed by anomalies of atria and interatrial communications (25.0%) and VSD (22.9%). 22q11.2 microdeletion was detected only in those with anomalies of extrapericardial arterial trunks (14.3%) or ventricular outflow tracts (6.4%). Conclusion ECM, chromosomal anomaly, and 22q11.2 microdeletion have different prevalence according to the type of CHD. © 2021 Public Library of Science. All rights reserved. | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | Public Library of Science | - |
dc.title | Prevalence of associated extracardiac anomalies in prenatally diagnosed congenital heart diseases | - |
dc.type | Article | - |
dc.identifier.doi | 10.1371/journal.pone.0248894 | - |
dc.identifier.bibliographicCitation | PLoS ONE, v.16, no.3 March | - |
dc.description.isOpenAccess | N | - |
dc.identifier.wosid | 000631029700041 | - |
dc.identifier.scopusid | 2-s2.0-85102899049 | - |
dc.citation.number | 3 March | - |
dc.citation.title | PLoS ONE | - |
dc.citation.volume | 16 | - |
dc.type.docType | Article | - |
dc.publisher.location | 미국 | - |
dc.subject.keywordPlus | 22q11.2 microdeletion | - |
dc.subject.keywordPlus | adult | - |
dc.subject.keywordPlus | Article | - |
dc.subject.keywordPlus | chromosome deletion | - |
dc.subject.keywordPlus | cohort analysis | - |
dc.subject.keywordPlus | congenital heart disease | - |
dc.subject.keywordPlus | disease association | - |
dc.subject.keywordPlus | female | - |
dc.subject.keywordPlus | heterotaxy syndrome | - |
dc.subject.keywordPlus | human | - |
dc.subject.keywordPlus | major clinical study | - |
dc.subject.keywordPlus | prenatal diagnosis | - |
dc.subject.keywordPlus | prevalence | - |
dc.subject.keywordPlus | retrospective study | - |
dc.subject.keywordPlus | valvular heart disease | - |
dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
dc.relation.journalWebOfScienceCategory | Multidisciplinary Sciences | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
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