![]() ![]() Distal aortopulmonary window with aortic origin of the right pulmonary artery and interruption of the aortic arch (Berry syndrome): diagnosis by MR imaging. Interruption of the aortic arch and coarctation of the aorta: Pathogenetic relations. Associated factors and trends in outcomes of interrupted aortic arch. Oosterhof T, Azakie A, Freedom RM, et al. Aortopulmonary window associated with interrupted aortic arch: report of surgical repair of eight cases and review of literature. Extensive collateral vessels are evident in the paraspinal region. IAA is associated with additional cardiovascular anatomic defects in up to 98 of the cases. Murin P, Sinzobahamvya N, Blaschczok HCH, et al. Computed tomography angiography revealed interrupted aortic arch type A, bivalve aorta, hemopericardium, aortic dissection Stanford A, and important collateral circulation. 1 Preoperative, contrast-enhanced, 3-dimensional, magnetic resonance angiogram (lateral view) reveals severe hypoplasia of the transverse aortic arch (arrow) between the origins of the left common carotid and left subclavian arteries (interrupted aortic arch, type B). Type C is seen when the ventral portion of the left third aortic arch and left fourth aortic arch involute, and there is a persistent ductus caroticus, a structure that normally regresses. Interrupted right aortic arch in DiGeroge syndrome. Moerman P, Dumoulin M, Lauweryns J, Van der Hauwaert LG. Repair of the truncal valve and associated interrupted arch in neonates with truncus arteriosus. Jahangiri M, Zurakowski D, Mayer JE, et al. Interrupted aortic arch is a rare and severe congenital heart defect characterized by a complete loss of luminal and anatomic continuity between the ascending. One-stage total repair of aortic arch anomaly using regional perfusion. Distal aortopulmonary septal defect, aortic origin of the right pulmonary artery, intact ventricular septum, patent ductus arteriosus and hypoplasia of the aortic isthmus: a newly recognized syndrome. ![]()
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