Rare association of absent pulmonary valve syndrome, complete atrioventricular canal defect, double outlet right ventricle, right aortic arch, and aberrant right subclavian artery in a fetal case.

Autor: Başar EZ; Department of Pediatric Cardiology, Faculty of Medicine, Kocaeli University, Kocaeli, Turkey., Doğan Y; Department of Perinatology, Faculty of Medicine, Kocaeli University, Kocaeli, Turkey., Şaşmazel A; Department of Pediatric Cardiovascular Surgery, Siyami Ersek Thoracic and Cardiovascular Surgery Education Research Hospital, Istanbul, Turkey., Babaoğlu K; Department of Pediatric Cardiology, Faculty of Medicine, Kocaeli University, Kocaeli, Turkey.
Jazyk: angličtina
Zdroj: Echocardiography (Mount Kisco, N.Y.) [Echocardiography] 2022 Oct; Vol. 39 (10), pp. 1359-1362. Date of Electronic Publication: 2022 Sep 20.
DOI: 10.1111/echo.15446
Abstrakt: Absent pulmonary valve syndrome (APVS) is a rare congenital cardiac anomaly. It is often associated with TOF, but may also be associated with an intact ventricular septum or, more rarely, with tricuspid atresia. It's combination with a complete atrioventricular septal defects and double outlet right ventricle has been reported extremely rare, even in the postnatal period. Herein, we report a 20-week-old fetus with a right aortic arch and an aberrant left subclavian artery with this rare combination. We report a case of a 20-week fetus diagnosed having this rare combination of right aortic arch and aberrant left subclavian artery. The APVS with complete atrioventricular septal defects may represent another type of APVS.
(© 2022 Wiley Periodicals LLC.)
Databáze: MEDLINE
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