Prenatal diagnosis and postnatal outcomes of right aortic arch anomalies

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dc.contributor.authorSelcuki, Nura Fitnat Topbas
dc.contributor.authorSenol, Gokalp
dc.contributor.authorEsin, Didem
dc.contributor.authorOzkose, Zeynep Gedik
dc.contributor.authorCaypinar, Sema Suzen
dc.contributor.authorBornaun, Helen
dc.contributor.authorCetin, Berna Arslan
dc.date.accessioned2024-03-13T10:30:42Z
dc.date.available2024-03-13T10:30:42Z
dc.date.issued2022
dc.departmentİstanbul Beykent Üniversitesien_US
dc.description.abstractPurpose To give a report on the experience of our tertiary perinatology clinic on the pre- and postnatal management of the right aortic arch (RAA) by evaluating the patients as isolated and non-isolated RAA. Materials and methods Patients referred to our perinatology clinic for fetal echocardiography were evaluated retrospectively. They were assessed in two groups: isolated RAA and non-isolated RAA. The isolated RAA group consisted of patients without any additional cardiac or extracardiac anomalies. According to our routine practice, all patients received detailed prenatal ultrasonography following fetal echocardiography and genetic counseling. Results A total of 60 patients were evaluated. 38 patients (63.3%) presented with additional cardiac anomalies. 21.7% had extracardiac anomalies, including 16.7% who also had cardiac anomalies. In 2 patients (3.7%) 22q11.2 microdeletion, in 2 patients (3.7%) trisomy 21, in 1 patient (1.9%) trisomy 13 and in 1 patient (1.9%) 20p12.1p11.23 (a deletion of 2880 kbp) were reported. The most common cardiac anomaly associated with RAA was Tetralogy of Fallot (25%). Fetal growth restriction was reported in 8.3% of the cases. 18 patients had isolated RAA. 16 out of the 18 patients had normal genetic analysis. 2 of them (11.11%) presented with a 22q11.2 microdeletion. Conclusion A single-center experience on the diagnosis and management of RAA has been reported in this study. The results indicate that a prenatal cardiac evaluation in 3VV is of utmost importance in all pregnancies to detect RAA and refer these patients to the appropriate perinatology clinics for further evaluation and care.en_US
dc.identifier.doi10.1007/s00404-021-06346-7
dc.identifier.endpage752en_US
dc.identifier.issn0932-0067
dc.identifier.issn1432-0711
dc.identifier.issue3en_US
dc.identifier.pmid34981204en_US
dc.identifier.scopus2-s2.0-85122175647en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage745en_US
dc.identifier.urihttps://doi.org/10.1007/s00404-021-06346-7
dc.identifier.urihttps://hdl.handle.net/20.500.12662/3503
dc.identifier.volume306en_US
dc.identifier.wosWOS:000737680600001en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherSpringer Heidelbergen_US
dc.relation.ispartofArchives Of Gynecology And Obstetricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectRight aortic archen_US
dc.subjectFetal echocardiographyen_US
dc.subjectCongenital heart diseaseen_US
dc.subject22q11en_US
dc.subject2 microdeletionen_US
dc.titlePrenatal diagnosis and postnatal outcomes of right aortic arch anomaliesen_US
dc.typeArticleen_US

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