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Don’t fight Congenitally corrected transposition of the great arteries alone.
Find your community on the free RareGuru App.Congenitally corrected transposition of the great arteries is a rare heart defect that occurs when the ventricles and attached valves are switched. As a result, the aorta and the pulmonary artery are connected to the wrong lower heart chambers. Click here to visit MayoClinic.com and view an image of this heart defect. While the oxygen-poor blood still flows to the lungs, and oxygen-rich blood still flows out to nourish the body, other heart problems (such as septal defects, pulmonary stenosis, tricuspid regurgitation, and heart block) are often associated with this defect and require treatment.
Source: GARD Last updated on 05-01-20
80%-99% of people have these symptoms.
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| Aortic atherosclerotic lesion |
| Thymus hyperplasia |
| Abnormal left ventricular outflow tract morphology |
| Discordant atrioventricular connection |
30%-79% of people have these symptoms.
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5%-29% of people have these symptoms.
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1%-4% of people have these symptoms.
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| Atrial flutter |
| Mesocardia |
| Ventricular tachycardia |
Currently the cause of congenitally corrected transposition of the great arteries is not known. Limited data suggests that air pollutants and hair dye may act as environmental risk factors for this rare defect. Also, having a family history of this heart defect is a risk factor. It has been estimated that the recurrence risk in siblings is around 3% to 5%.
Last updated on 05-01-20
You can view an Image of congenitally corrected transposition of the great vessels on the MayoClinic.com Web site. To view click on "Image" above.
Last updated on 04-27-20
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