Subpulmonary Stenosis Assessed in Midtrimester Fetuses With Tetralogy of Fallot: A Novel Method for Predicting Postnatal Clinical Outcome

2013 ◽  
Vol 34 (6) ◽  
pp. 1314-1320 ◽  
Author(s):  
Elena N. Kwon ◽  
Ira A. Parness ◽  
Shubhika Srivastava ◽  
James C. Nielsen ◽  
Miwa Geiger
2011 ◽  
Vol 3 (1) ◽  
pp. 100
Author(s):  
Maxime De Guillebon ◽  
Pierre Bordachar ◽  
Xavier Iriart ◽  
Philippe Ritter ◽  
Alice Horovitz ◽  
...  

2005 ◽  
Vol 15 (S1) ◽  
pp. 38-47 ◽  
Author(s):  
Robert H. Anderson ◽  
Paul M. Weinberg

It is now well over one hundred years since Arthur Louis Etienne Fallot showed that four discrete morphologic abnormalities co-existed in the majority of patients he had autopsied with “la maladie bleu”,1 or cyanosis as we now describe it. The lesions he identified were an interventricular communication, subpulmonary stenosis, biventricular origin of the aortic valve, and right ventricular hypertrophy. We now know that the combination of these anomalies had been recognised long before Fallot's epochal description. Indeed, it is Neils Stensen, the Danish monk who also described the parotid duct, who is usually acknowledged as being the first to describe the entity that we now call tetralogy of Fallot.2 Cases were certainly described by John Hunter,2 whilst with the benefit of hindsight, we can see an unequivocal example illustrated by the Baron von Rokitansky3 in his ground-breaking atlas (Fig. 1).


1989 ◽  
Vol 47 (3) ◽  
pp. 428-435 ◽  
Author(s):  
Giovaani Calza ◽  
Giuseppe Panizzon ◽  
Salvatore Rovida ◽  
Jacques Aigueperse

2013 ◽  
Vol 23 (6) ◽  
pp. 858-866 ◽  
Author(s):  
Robert H. Anderson ◽  
Diane E. Spicer ◽  
Jorge M. Giroud ◽  
Timothy J. Mohun

AbstractIt is timely, in the 125th anniversary of the initial description by Fallot of the hearts most frequently seen in patients presenting with “la maladie bleu”, that we revisit his descriptions, and discuss his findings in the light of ongoing controversies. Fallot described three hearts in his initial publication, and pointed to the same tetralogy of morphological features that we recognise today, namely, an interventricular communication, biventricular connection of the aorta, subpulmonary stenosis, and right ventricular hypertrophy. In one of the hearts, he noted that the aorta arose exclusively from the right ventricle. In other words, one of his initial cases exhibited double-outlet right ventricle. When we now compare findings in hearts with the features of the tetralogy, we can observe significant variations in the nature of the borders of the plane of deficient ventricular septation when viewed from the aspect of the right ventricle. We also find that this plane, usually described as the ventricular septal defect, is not the same as the geometric plane separating the cavities of the right and left ventricles. This means that the latter plane, the interventricular communication, is not necessarily the same as the ventricular septal defect. We are now able to provide further insights into these features by examining hearts prepared from developing mice. Additional molecular investigations will be required, however, to uncover the mechanisms responsible for producing the morphological changes underscoring tetralogy of Fallot.


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