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Konstantinov, I.E., Karamlou, T., Williams, W.G., et al. (2006) Surgical Management of Aortopulmonary Window Associated with Interrupted Aortic Arch: A Congenital Heart Surgeons Society Study. The Journal of Thoracic and Cardiovascular Surgery, 131, 1136-1141e2.
https://doi.org/10.1016/j.jtcvs.2005.03.051

has been cited by the following article:

• TITLE: Aorto-Pulmonary Window, an Unrecognized Cause of Heart Failure in Infants: A Case Report

  AUTHORS: Mohammed Ech-Chebab, Ayyad Ghannam, Aziza El Ouali, Maria Rkain, Noufissa Benajiba, Abdeladim Babakhouya

  KEYWORDS: Aorto-Pulmonary Window, Heart Failure, Infant, Congenital

  JOURNAL NAME: World Journal of Cardiovascular Diseases, Vol.10 No.9, September 25, 2020

  ABSTRACT: Introduction: The aorto-pulmonary window is a rare congenital heart disease. It is a defect between the ascending aorta and the trunk of the pulmonary artery upstream of the pulmonary bifurcation. Once the diagnosis is made, surgery must be performed quickly to avoid progression to pulmonary arteriolitis. We report the case of a 4-month-old infant in whom we made the diagnosis of aorto-pulmonary window type I. He was able to benefit from an open heart surgery at FES with an excellent result after closing the window. Conclusion: The aorto-pulmonary window is a rare congenital heart defect, the diagnosis of which must be made as early as possible in order to avoid the progression to pulmonary hypetension and heart failure.