Nonsyndromic genetic predisposition to aortic dissection: a newly recognized, diagnosable, and preventable occurrence in families

Ann Emerg Med. 2004 Jan;43(1):79-82. doi: 10.1016/s0196-0644(03)00818-7.

Abstract

The major diseases affecting the aorta are aortic aneurysms and dissections, with patients with acute dissections often presenting in the emergency department (ED). Recent studies demonstrate a strong genetic predisposition to thoracic aortic aneurysms and dissections, independent of syndromes traditionally considered to predispose to aortic disease (such as Marfan syndrome). Nonsyndromic familial thoracic aortic aneurysms and dissections are inherited in families as an autosomal dominant disorder and a variable age of onset of the aortic disease. The case reported here illustrates the critical importance of obtaining a family history of thoracic aortic aneurysms and dissections, along with unexplained sudden death, when assessing an individual with chest pain in the ED, regardless of age and in the absence of a known genetic syndrome.

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Aortic Aneurysm, Thoracic / diagnosis*
  • Aortic Aneurysm, Thoracic / epidemiology
  • Aortic Aneurysm, Thoracic / genetics*
  • Aortic Dissection / diagnosis*
  • Aortic Dissection / epidemiology
  • Aortic Dissection / genetics*
  • Chest Pain / diagnosis
  • Chest Pain / epidemiology
  • Chromosome Mapping
  • Diagnosis, Differential
  • Emergency Medicine / methods
  • Emergency Service, Hospital*
  • Family*
  • Female
  • Genetic Predisposition to Disease* / epidemiology
  • Genetic Predisposition to Disease* / genetics
  • Humans
  • Male
  • Medical History Taking
  • Pedigree