Aortopathy in Congenital Heart Disease

Timothy B. Cotts, Katherine B. Salciccioli, Sara K. Swanson, Anji T. Yetman

Research output: Contribution to journalReview article

Abstract

Aortic dilatation is common in patients with congenital heart disease and is seen in patients with bicuspid aortic valve and those with conotruncal congenital heart defects. It is important to identify patients with bicuspid aortic valve at high risk for aortic dissection. High-risk patients include those with the aortic root phenotype and those with syndromic or familial aortopathies including Marfan syndrome, Loeys-Dietz syndrome, and Turner syndrome. Aortic dilatation is common in patients with conotruncal congenital heart defects and rarely results in aortic dissection.

Original languageEnglish (US)
Pages (from-to)325-336
Number of pages12
JournalCardiology Clinics
Volume38
Issue number3
DOIs
StatePublished - Aug 2020

Keywords

  • Aortic dissection
  • Aortopathy
  • Bicuspid aortic valve
  • Congenital heart disease

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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