{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T03:37:46Z","timestamp":1790739466676,"version":"4.1.0"},"reference-count":10,"publisher":"Oxford University Press (OUP)","issue":"2","license":[{"start":{"date-parts":[[2020,6,15]],"date-time":"2020-06-15T00:00:00Z","timestamp":1592179200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2020,8,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Aberrant subclavian artery (arteria lusoria) is the most common congenital malformation of the aortic arch in the general population. As patients are more often asymptomatic, indications for correcting this abnormality, even in those having dysphagia, are very vague. While presenting a case of a 10-year-old girl who suffered from dysphagia lusoria for 2\u2009years before being cured by a simple surgical translocation, we review the literature and debate various aspects of its management from diagnosis to surgery and cosmesis.<\/jats:p>","DOI":"10.1093\/icvts\/ivaa091","type":"journal-article","created":{"date-parts":[[2020,4,29]],"date-time":"2020-04-29T11:12:17Z","timestamp":1588158737000},"page":"228-231","source":"Crossref","is-referenced-by-count":14,"title":["Dysphagia and an aberrant subclavian artery: more than just a coincidence"],"prefix":"10.1093","volume":"31","author":[{"given":"Vilius","family":"Dranseika","sequence":"first","affiliation":[{"name":"Congenital Cardiovascular Surgery, Children\u2019s Heart Centre and Children\u2019s Research Centre, University Children\u2019s Hospital Zurich, Zurich, 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