Prevalence and Types of Aortic Arch Variants and Anomalies in Congenital Heart Diseases

2019 ◽  
Vol 26 (7) ◽  
pp. 930-936 ◽  
Author(s):  
Ahmed M. Tawfik ◽  
Donia M. Sobh ◽  
Germeen A. Ashamallah ◽  
Nihal M. Batouty
2020 ◽  
Vol 23 (4) ◽  
pp. E507-E509
Author(s):  
Huang Feng ◽  
Xiaohui Bian ◽  
Yuru Lan ◽  
Yunfei Ling ◽  
Yong jun Qian

Double aortic arch (DAA) is an extremely rare congenital anomaly that can be divided into right dominant, left dominant, and balanced DAA according to the relative size of the two arches. The incidence of balanced DAA is only 5% among double arch anomalies. DAA is symptomatic only when it produces symptoms secondary to compression of the trachea or esophagus. DAA is rarely associated with other congenital heart diseases. In this report, we present a rare case of asymptomatic DAA combined with Tetralogy of Fallot (TOF) in an 8-month-old girl.


2013 ◽  
Vol 15 (1) ◽  
pp. 101 ◽  
Author(s):  
Hopewell N Ntsinjana ◽  
Giovanni Biglino ◽  
Claudio Capelli ◽  
Oliver Tann ◽  
Alessandro Giardini ◽  
...  

1994 ◽  
Vol 4 (2) ◽  
pp. 187-189
Author(s):  
Beth Bubolz ◽  
Christopher L. Case ◽  
Robert M. Sade

SummarySummary Absence of the arterial duct has been reported in association with tetralogy of Fallot, with pulmonary stenosis or atresia, other complex cyanotic congenital heart diseases, and anomalies of the aortic arch but not, as far as we are aware, with tricuspid atresia. We report the clinical, surgical, and autopsy findings of a patient with tricuspid atresia whose initial clinical course was influenced by the absence of thearterial duct.


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