<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(11)</volume><submitter>Van den Eynde J</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Coronary anomalies are present in one-third of all patients with transposition of the great arteries (TGA) and have been associated with increased risk of adverse outcomes after the arterial switch operation. Therefore, knowledge about coronary anatomy remains key.&lt;h4>Case summary&lt;/h4>A 5-day-old girl with prenatal diagnosis of Taussig-Bing anomaly (double outlet right ventricle with TGA and large subpulmonary ventricular septal defect) along with aortic arch hypoplasia and coarctation of the aorta underwent the arterial switch operation with closure of the ventricular septal defect and aortic arch repair. On preoperative echocardiography, the right (R) and left coronary artery (LCx) connected both to aortic sinus 1, suggesting 1RLCx coronary anatomy according to the Lei</pubmed_abstract><journal>European heart journal. Case reports</journal><pagination>ytac432</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9645565</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Anomalous connection of the circumflex coronary artery to the pulmonary trunk in a patient with Taussig-Bing anomaly: a case report.</pubmed_title><pmcid>PMC9645565</pmcid><pubmed_authors>Hazekamp MG</pubmed_authors><pubmed_authors>Van den Eynde J</pubmed_authors><pubmed_authors>Jongbloed MRM</pubmed_authors><pubmed_authors>van der Palen RLF</pubmed_authors><pubmed_authors>Rammeloo LAJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Anomalous connection of the circumflex coronary artery to the pulmonary trunk in a patient with Taussig-Bing anomaly: a case report.</name><description>&lt;h4>Background&lt;/h4>Coronary anomalies are present in one-third of all patients with transposition of the great arteries (TGA) and have been associated with increased risk of adverse outcomes after the arterial switch operation. Therefore, knowledge about coronary anatomy remains key.&lt;h4>Case summary&lt;/h4>A 5-day-old girl with prenatal diagnosis of Taussig-Bing anomaly (double outlet right ventricle with TGA and large subpulmonary ventricular septal defect) along with aortic arch hypoplasia and coarctation of the aorta underwent the arterial switch operation with closure of the ventricular septal defect and aortic arch repair. On preoperative echocardiography, the right (R) and left coronary artery (LCx) connected both to aortic sinus 1, suggesting 1RLCx coronary anatomy according to the Lei</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-25T19:35:25.689Z</modification><creation>2025-04-06T08:01:15.091Z</creation></dates><accession>S-EPMC9645565</accession><cross_references><pubmed>36381175</pubmed><doi>10.1093/ehjcr/ytac432</doi></cross_references></HashMap>