{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,16]],"date-time":"2026-07-16T12:19:34Z","timestamp":1784204374482,"version":"3.55.0"},"reference-count":29,"publisher":"Walter de Gruyter GmbH","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,3,25]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec id=\"j_jpm-2023-0410_abs_001\">\n                  <jats:title>Objectives<\/jats:title>\n                  <jats:p>Right aortic arch (RAA) is a rare anomaly with an incidence of 0.1\u202f% in the adult population and low-risk fetuses. Our aim in this study was to evaluate associated anomalies and conditions according to subtypes.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec id=\"j_jpm-2023-0410_abs_002\">\n                  <jats:title>Methods<\/jats:title>\n                  <jats:p>This was a retrospective study examining consecutive pregnancies diagnosed with RAA in our hospital between 2018 and 2022. Fetuses with RAA were divided into three groups, RAA with right-sided ductus arteriosus (RAA-RDA), RAA with left-sided ductus arteriosus (RAA-LDA), and RAA with a double aortic arch (RAA-DAA).<\/jats:p>\n               <\/jats:sec>\n               <jats:sec id=\"j_jpm-2023-0410_abs_003\">\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>A total of 81 fetuses were diagnosed as having RAA during the study period. The rate of cardiac anomalies (82.8\u202f%) in the RAA-RDA group was higher than in the RAA-LDA (17.6\u202f%) and RAA-DAA (22.2\u202f%) groups (p&lt;0.001). No statistically significant difference was found between the groups in terms of maternal age, diagnosis week, pregnancy outcome, extracardiac anomalies, and genetic anomalies. Three (8\u202f%) of 36 fetuses with isolated RAA who resulted in live birth developed symptoms related to the vascular ring, and one (2.7\u202f%) newborn with RAA-DAA underwent surgery.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec id=\"j_jpm-2023-0410_abs_004\">\n                  <jats:title>Conclusions<\/jats:title>\n                  <jats:p>The incidence of cardiac anomalies is high in fetuses with RAA-RDA. Ultrasound examinations should be performed for cardiac anomalies and additional structural anomalies. Vascular ring formation is a rare but important complication due to compression risk to the trachea and esophagus.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1515\/jpm-2023-0410","type":"journal-article","created":{"date-parts":[[2024,1,27]],"date-time":"2024-01-27T14:10:33Z","timestamp":1706364633000},"page":"304-309","source":"Crossref","is-referenced-by-count":2,"title":["Prenatal diagnosis of right aortic arch: associated anomalies and fetal prognosis according to different subtypes"],"prefix":"10.1515","volume":"52","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7255-860X","authenticated-orcid":false,"given":"Gizem Elif","family":"Dizdaro\u011fullar\u0131","sequence":"first","affiliation":[{"name":"Department of Perinatology, Kartal Dr. Lutfi K\u0131rdar City Hospital , Health Science University , Istanbul , T\u00fcrkiye"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Abdullah","family":"Alp\u0131nar","sequence":"additional","affiliation":[{"name":"Department of Pediatric Cardiology, Zeynep Kamil Women and Children\u2019s Diseases Training and Research Hospital , Health Science University , Istanbul , T\u00fcrkiye"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Oya","family":"Demirci","sequence":"additional","affiliation":[{"name":"Department of Perinatology, Zeynep Kamil Women and Children\u2019s Diseases Training and Research Hospital , Health Science University , Istanbul , T\u00fcrkiye"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"374","published-online":{"date-parts":[[2024,1,29]]},"reference":[{"key":"2024030611333440533_j_jpm-2023-0410_ref_001","doi-asserted-by":"crossref","unstructured":"Li, S, Luo, G, Norwitz, ER, Wang, C, Ouyang, S, Yao, Y, et al.. Prenatal diagnosis of congenital vascular rings and slings: sonographic features and perinatal outcome in 81 consecutive cases. Prenat Diagn 2011;31:334\u201346. https:\/\/doi.org\/10.1002\/pd.2678.","DOI":"10.1002\/pd.2678"},{"key":"2024030611333440533_j_jpm-2023-0410_ref_002","doi-asserted-by":"crossref","unstructured":"Li, S, Wen, H, Liang, M, Luo, D, Qin, Y, Liao, Y, et al.. Congenital abnormalities of the aortic arch: revisiting the 1964 Stewart classification. Cardiovasc Pathol 2019;39:38\u201350. https:\/\/doi.org\/10.1016\/j.carpath.2018.11.004.","DOI":"10.1016\/j.carpath.2018.11.004"},{"key":"2024030611333440533_j_jpm-2023-0410_ref_003","doi-asserted-by":"crossref","unstructured":"Evans, WN, Acherman, RJ, Ciccolo, ML, Carrillo, SA, Mayman, GA, Luna, CF, et al.. Vascular ring diagnosis and management: notable trends over 25 years. 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