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. |
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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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