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Mid-aortic syndrome diagnosed by transesophageal echocardiogram in a patient with dilated cardiomyopathy
Benjamin W Theisen1,2, Kenneth R Knecht1,2, Joshua A Daily1,2
1Arkansas Children's Hospital, Little Rock, AR, USA.
Mid-aortic syndrome is a rare condition characterised by segmental narrowing of the thoracoabdominal aorta. Here, we demonstrate a case of mid-aortic syndrome in a 30-month-old female who was diagnosed via transesophageal echocardiography after presenting with dilated cardiomyopathy and severe heart failure requiring placement of a left ventricular assist device.
Mid-aortic syndrome is a rare condition characterised by segmental narrowing of the thoracoabdominal aorta. Here, we demonstrate a case of mid-aortic syndrome in a 30-month-old female who was diagnosed via transesophageal echocardiography after presenting with dilated cardiomyopathy and severe heart failure requiring placement of a left ventricular assist device.
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