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Right-sided aortic arch is a rare anatomical variant in which the aortic arch is on the right side rather than on the left. During normal embryonic development, the aortic arch is formed by the left fourth aortic arch and the left dorsal aorta. In people with a right-sided aortic arch, instead the right dorsal aorta persists and the distal left ...
A double aortic arch; occurs with the development of an abnormal right aortic arch in addition to the left aortic arch, forming a vascular ring around the trachea and esophagus, which usually causes difficulty breathing and swallowing. Occasionally, the entire right dorsal aorta abnormally persists and the left dorsal aorta regresses in which ...
The aortic arch is the connection between the ascending and descending aorta, and its central part is formed by the left 4th aortic arch during early development. [12] The ductus arteriosus connects to the lower part of the arch in foetal life. This allows blood from the right ventricle to mostly bypass the pulmonary vessels as they develop.
It is the first branch of the aortic arch. [3] Soon after it emerges, the brachiocephalic artery divides into the right common carotid artery and the right subclavian artery. [4] There is no brachiocephalic artery for the left side of the body. The left common carotid artery and the left subclavian artery come directly off the aortic arch.
The right coronary artery supplies oxygenated blood to the right atrium, the right ventricle, and the posterior third and inferior end of the interventricular septum. [2] [5] It may also supply 25% to 35% of the left ventricle (LV). [10] There is significant overlap of supply of the coronary arteries. [2]
Isolated double aortic arch without associated intracardiac defects is a vascular anomaly that can be corrected without the support of cardiopulmonary bypass. [citation needed] For surgical division of the narrower left aortic arch in a typical double arch patient with a dominant right arch, the patient is placed on the right side.
right-sided aortic arch, in 25%; coronary artery anomalies, in 10%; a patent foramen ovale or atrial septal defect, in which case the syndrome is sometimes called a pentalogy of Fallot [46] an atrioventricular septal defect; partially or totally anomalous pulmonary venous return
Coarctation of the aorta (CoA) – Narrowing of the aorta, typically of the aortic arch and is classically found in Turner syndrome. A "complete" coarction is called an interrupted aortic arch. Cor triatriatum – A membrane that divides one of the atria results in "three" atria (hence "triatriatum"). This tends to affect the left atrium more ...
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