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Atrial septal defect (ASD) is a congenital heart defect in which blood flows between the atria (upper chambers) of the heart. Some flow is a normal condition both pre-birth and immediately post-birth via the foramen ovale ; however, when this does not naturally close after birth it is referred to as a patent (open) foramen ovale (PFO).
An Atrial septal defect is a relatively common heart malformation that occurs when the interatrial septum fails to develop properly. Persistence of the ostium secundum is the most common atrial septal defect. [3] Additionally, in a subset of the population, the foramen ovale is not overtly patent but the two septa have not fused.
This pouch can protrude into the right atrium or the left atrium. The cause of this aneurysm is the result of abnormal, increased pressure within the heart. Even if the foramen ovale does seal shut, an aneurysm may occur, usually on the side of the right atrium. If the aneurysm stretches too far, it can narrow the opening of the inferior vena ...
Atrial septal defect with left-to-right shunt. The left and right sides of the heart are named from a dorsal view, i.e., looking at the heart from the back or from the perspective of the person whose heart it is. There are four chambers in a heart: an atrium (upper) and a ventricle (lower) on both the left and right sides. [1]
A VSD can cause a left-to-right shunt of blood flow in the heart and is one of the most common of the congenital heart defects. This type of shunt is an acyanotic disorder that can result in ventricular hypertrophy. [4] The alignment of interventricular septum and interatrial septum is disturbed in various congenital heart diseases. [5]
Failure of the septum primum to fuse with the endocardial cushion can lead to an ostium primum atrial septal defect. [1] This is the second most common type of atrial septal defect [2] and is commonly seen in Down syndrome. Typically, this defect will cause a shunt to occur from the left atrium to the right atrium.
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Eisenmenger syndrome or Eisenmenger's syndrome is defined as the process in which a long-standing left-to-right cardiac shunt caused by a congenital heart defect (typically by a ventricular septal defect, atrial septal defect, or less commonly, patent ductus arteriosus) causes pulmonary hypertension [1] [2] and eventual reversal of the shunt into a cyanotic right-to-left shunt.
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