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Aortopulmonary septal defect information


Aortopulmonary septal defect
SpecialtyCardiology

Aortopulmonary septal defect is a rare congenital heart disorder accounting for only 0.1-0.3% of congenital heart defects worldwide.[1] It is characterized by a communication between the aortic and pulmonary arteries, with preservation of two normal semilunar valves. It is the result of an incomplete separation of the aorticopulmonary trunk that normally occurs in early fetal development with formation of the spiral septum.[2] Aortopulmonary septal defects occur in isolation in about half of cases, the remainder are associated with more complex heart abnormalities.[3]

  1. ^ Love, Barry (5 February 2015). "Aortopulmonary Septal Defect". Medscape.
  2. ^ Burakovsky, V. I., Falkovsky, G. E., & Ivanitsky, A. V. (1984). Surgical repair of truncus arteriosus. Pediatric cardiology, 5(2), 111-114.
  3. ^ McElhinney DB, Reddy VM, Tworetzky W, Silverman NH, Hanley FL (January 1998). "Early and late results after repair of aortopulmonary septal defect and associated anomalies in infants <6 months of age". Am. J. Cardiol. 81 (2): 195–201. doi:10.1016/S0002-9149(97)00881-3. PMID 9591904.

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