Repair of Bicuspid Aortic Valve Syndrome with Anomalous Right Coronary Artery in Osteogenesis Imperfecta.

Published

Journal Article

Osteogenesis imperfecta (OI) is an inherited connective tissue disorder caused by the defective synthesis of type I collagen. The clinical phenotype is dominated by bone fragility, but cardiovascular tissue involvement has also been reported. Here, the case is described of a 37-year-old man with OI who presented with aortic insufficiency, bicuspid aortic valve, dilated aortic root, and anomalous right coronary artery. The patient was treated successfully with a mechanical valved conduit aortic root replacement and anomalous coronary artery unroofing and reimplantation. This case highlights the feasibility of complex surgical repairs in this population, as well as challenges surrounding the choice of valve prosthesis given the congenital bone fragility and predilection for fractures.

Full Text

Duke Authors

Cited Authors

  • Davis, RP; Andersen, ND; Ganapathi, AM; DiBernardo, LR; Hughes, GC

Published Date

  • November 2015

Published In

Volume / Issue

  • 24 / 6

Start / End Page

  • 666 - 668

PubMed ID

  • 27997768

Pubmed Central ID

  • 27997768

International Standard Serial Number (ISSN)

  • 0966-8519

Language

  • eng

Conference Location

  • England