Anomalous origin of the left coronary artery from the dorsal aortic sinus and its relationship with aortic valve morphology in Syrian hamsters

1995 ◽  
Vol 112 (4) ◽  
pp. 373-380 ◽  
Author(s):  
M. Cardo ◽  
B. Fernández ◽  
A.C. Durán ◽  
M.C. Fernández ◽  
J.M. Arqué ◽  
...  
2006 ◽  
Vol 134 (4) ◽  
pp. 290-296 ◽  
Author(s):  
A.C. Durán ◽  
T. Fernández-Gallego ◽  
B. Fernández ◽  
M.C. Fernández ◽  
J.M. Arqué ◽  
...  

2020 ◽  
Vol 30 (7) ◽  
pp. 1046-1049 ◽  
Author(s):  
Sharmeen Samuel ◽  
Preeta Dhanantwari ◽  
Nilanjana Misra ◽  
David B. Meyer

AbstractIsolated aortic regurgitation and myocardial infarction are a rare congenital defect among neonatal patients. We present a case of a neonate with an unusual aortic valve morphology causing both regurgitation and obstruction of the left coronary artery ostium. Despite both non-invasive and invasive imaging modalities, accurate diagnosis of the valve morphology was only determined by direct visualisation at the time of surgical repair. To the knowledge of authors, this particular aortic valve morphology in neonatal population has not been previously reported in the literature.


2000 ◽  
Vol 34 (2) ◽  
pp. 145-154 ◽  
Author(s):  
M. C. Fernández ◽  
A. C. Durán ◽  
R. Real ◽  
D. López ◽  
B. Fernández ◽  
...  

In the Syrian hamster, anomalies in the origin of the left coronary artery are significantly associated with the bicuspid condition of the aortic valve. In this species, bicuspid aortic valves are expressions of a trait, the variation of which takes the form of a phenotypic continuum, ranging from a tricuspid aortic valve with no commissural fusion to a bicuspid aortic valve with the aortic sinuses located in ventrodorsal orientation and devoid of any raphe. The intermediate stages of the continuum are represented by tricuspid aortic valves with a more or less extensive fusion of the ventral commissure and bicuspid aortic valves with a more or less developed raphe located in the ventral aortic sinus. The present study was designed to decide whether there is a gap between tricuspid and bicuspid aortic valves regarding the incidence of coronary artery anomalies, or whether this incidence varies according to the different tricuspid and bicuspid morpho types of the continuum. The study was carried out in Syrian hamsters belonging to a single inbred family with a high incidence of tricuspid aortic valves with fusion of the ventral commissure, bicuspid aortic valves, and anomalies in the origin of the left coronary artery, i.e. single right coronary artery ostium in aorta, anomalous origin of the left coronary artery from the pulmonary artery, and anomalous origin of the left coronary artery from the dorsal aortic sinus. The specimens were examined by means of a stereomicroscope and, in several cases; scanning electron microscopy was also used. The relationships between anomalous coronary artery patterns and aortic valve morphologies were tested using a logistic regression model. The results obtained indicate that there is no discontinuity between tricuspid and bicuspid aortic valves regarding the incidence of coronary artery anomalies. The probability of occurrence of anomalous coronary artery patterns increases continuously according to the deviation degree of the aortic valve from its normal (tricuspid) design. The present findings suggest that in the Syrian hamster, the morphogenetic mechanisms involved in the formation of congenital anomalous aortic valves and anomalies in the origin of the left coronary artery, respectively, are strongly related from an aetiological viewpoint.


2002 ◽  
Vol 12 (1) ◽  
pp. 78-80 ◽  
Author(s):  
Tony Abdel Massih ◽  
Sally-Ann B. Clur ◽  
Philipp Bonhoeffer

We report a 12-year-old child with anomalous origin of the left coronary artery from the right coronary aortic sinus, the artery taking a proximal intramural course. The anomalous artery was reimplanted into the left coronary aortic sinus. Postoperative stenosis was successfully treated with percutaneous transluminal angioplasty and implantation of a stent.


2005 ◽  
Vol 15 (2) ◽  
pp. 213-215 ◽  
Author(s):  
Masayuki Morikawa ◽  
Ko Bando ◽  
Shinji Sato

We treated successfully using the Ross procedure a 14-year old with a congenitally stenotic bifoliate aortic valve associated with anomalous origin of the right coronary artery. The anomalous artery arose from the same aortic sinus that gave rise to the main stem of the left coronary artery, and reached the right atrioventricular groove by traversing the tissue plane between the aortic root and the subpulmonary infundibulum. Both coronary arteries were reimplanted using a single arterial button.


1993 ◽  
Vol 2 (1) ◽  
pp. 35-39 ◽  
Author(s):  
Josep M. Arqué ◽  
Gaetano Thiene ◽  
Manuel Cardo ◽  
Diego Franco ◽  
Ana C. Durán ◽  
...  

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