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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.
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 ...
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 ...
Another system divides the aorta with respect to its course and the direction of blood flow. In this system, the aorta starts as the ascending aorta, travels superiorly from the heart, and then makes a hairpin turn known as the aortic arch. Following the aortic arch, the aorta then travels inferiorly as the descending aorta. The descending ...
Double aortic arch is a subtype of complete vascular ring. There are three types of double aortic arch: Right dominant arch (about 70% of surgical cases) Balanced or codominant (about 5%): both arches are of equal size; Left dominant (about 25%) Double aortic arch with right dominant arch: Normally there is only
The two coronary arteries of the heart arise from the aortic root, just above the cusps of the aortic valve. The aorta then arches back over the right pulmonary artery. Three vessels come out of the aortic arch: the brachiocephalic artery, the left common carotid artery, and the left subclavian artery.
Interrupted aortic arch is a very rare heart defect (affecting 3 per million live births) [1] in which the aorta is not completely developed. There is a gap between the ascending and descending thoracic aorta .
Most are located above the aortic arch, [2] while some are located on the posterior side of the aortic arch between it and the pulmonary artery below. [3] They consist of glomus cells and sustentacular cells. [1] Some sources equate the "aortic bodies" and "paraaortic bodies", while other sources explicitly distinguish between the two.
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