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Aortic regurgitation (AR), also known as aortic insufficiency (AI), is the leaking of the aortic valve of the heart that causes blood to flow in the reverse direction during ventricular diastole, from the aorta into the left ventricle. As a consequence, the cardiac muscle is forced to work harder than normal.
Fetal aortic stenosis is a disorder that occurs when the fetus’ aortic valve does not fully open during development. [1] The aortic valve is a one way valve that is located between the left ventricle and the aorta , keeping blood from leaking back into the ventricle. [ 1 ]
Just like aortic stenosis, treatment for aortic regurgitation is replacement of the valve after symptoms and left ventricular dysfunction develops. SUMMARY All right, as a quick recap…. Aortic stenosis happens if the aortic valve doesn’t open all the way, and aortic valve regurgitation happens if the valve doesn’t close all the way.
They may protrude into the orifice of the mitral valve, leading to fixed obstruction of blood flow from the left atria to the left ventricles. [1] Subaortic stenosis has been observed in both muscular and membranous forms. In either case, a variable degree of obstruction may be observed at the ventricular surface of the aortic valve. [1]
The common artery, now separated from the pulmonary circulation, functions as the aorta with the truncal valve operating as the aortic valve. Most babies survive this surgical repair, but may require further surgery as they grow up. For example, the conduit does not grow with the child and may need to be replaced as the child grows.
The aortic valve normally has three cusps or leaflets, although in 1–2% of the population it is found to congenitally have two leaflets. [1] The aortic valve is the last structure in the heart the blood travels through before stopping the flow through the systemic circulation. [1]
Aortic regurgitation, on the other hand, has many causes: degeneration of the cusps, endocarditis, bicuspid aortic valve, aortic root dilatation, trauma, connective tissue disorders such as Marfan syndrome or Ehlers-Danlos lead to imperfect closure of the valve during diastole, hence the blood is returning from the aorta towards the left ...
The severity of symptoms depends on the type of TGV, and the type and size of other heart defects that may be present (ventricular septal defect, atrial septal defect, or patent ductus arteriosus). Most babies with TGA have blue skin color (cyanosis) in the first hours or days of their lives, since dextro-TGA is the more common type.