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Cardiovascular surgery in children with Marfan syndrome or Loeys-Dietz syndrome
The Journal of Thoracic and Cardiovascular Surgery, 04/14/09
Everitt MD et al. - Patients with Marfan or Loeys-Dietz syndrome requiring surgery during childhood have a favorable long-term outcome. Those undergoing valve-sparing root replacement or mitral valve repair have a low risk for reoperation. Postoperative angiotensin-converting enzyme inhibitor therapy confers clinical benefit.
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