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Role of Clinical Genetic Testing in the Management of Aortopathies.

Stephanie L HarrisMark E Lindsay
Published in: Current cardiology reports (2021)
Thoracic aortic disease may be non-syndromic or seen as part of a genetic syndrome, such as Marfan syndrome, Loeys-Dietz syndrome, or vascular Ehlers-Danlos syndrome. Expanded access to genetic testing has revealed the wide and overlapping phenotypic spectrum of these conditions, highlighting the need for genetic testing to establish an accurate diagnosis. Important aspects of genetic evaluation include thorough phenotyping through family history and physical examination, selection of an appropriate genetic test driven by the patient's phenotype, and careful interpretation of genetic test results. Improved understanding of the natural history of these conditions has led to tailored management recommendations, including gene-based recommendations for prophylactic surgical repair. Identification of a genetic etiology allows for careful monitoring of disease progression, informs the timing of prophylactic surgical repair, and facilitates the identification of other at-risk relatives through cascade genetic testing.
Keyphrases
  • genome wide
  • case report
  • copy number
  • heart failure
  • mental health
  • physical activity
  • aortic valve
  • spinal cord injury
  • gene expression
  • left ventricular
  • pulmonary hypertension
  • genome wide identification
  • light emitting