{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,2]],"date-time":"2026-06-02T15:40:15Z","timestamp":1780414815351,"version":"3.54.1"},"reference-count":32,"publisher":"Wiley","issue":"13","license":[{"start":{"date-parts":[[2018,12,16]],"date-time":"2018-12-16T00:00:00Z","timestamp":1544918400000},"content-version":"vor","delay-in-days":15,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["obgyn.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Prenatal Diagnosis"],"published-print":{"date-parts":[[2018,12]]},"abstract":"<jats:p>What is already known about the topic?\n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>Right aortic arch (RAA) has an association with extracardiac and chromosomal anomalies.<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>RAA with left arterial duct can form a vascular ring.<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>In children with RAA, there is poor correlation of symptoms and tracheal compression.<\/jats:p><\/jats:list-item>\n<\/jats:list><\/jats:p><jats:p>What does this study add?\n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>The majority of prenatal cases of an isolated RAA in our cohort are identified during routine screening.<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>Microdeletion of chromosome 22q11 is the most common genetic association with an apparently isolated RAA, it is seen in a minimum of 7% of cases.<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>A chromosomal or genetic anomaly is found in half of fetuses with RAA and increased nuchal translucency thickness (NT) and in one\u2010fifth of those with normal 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