Tags Archives: congenital cardiopathies

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Transposition of the great arteries (TGA) is a pediatric cardiac congenital defect arising from an embryological discordance between the aorta and pulmonary trunk. During cardiac development, the conotruncal septum spirals..

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Taussig-Bing anomaly is a rare congenital heart malformation that was first described in 1949 by Helen B. Taussig (1898–1986) and Richard J. Bing (1909–). Although substantial improvement has since been..

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Double outlet right ventricle (DORV) is a heterogeneous group of abnormal ventriculoarterial connections where, by definition, both great arteries (pulmonary artery and aorta) arise primarily from the morphologically right ventricle...

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Double-outlet right ventricle (DORV) and subaortic ventricular septal defect (VSD) is defined anatomically as a defect where the entire pulmonary trunk and at least half of the aorta arises from..

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The clinical, hemodynamic, angiocardiographic and pathologic findings are presented in an infrequent but surgically correctable type of double outlet right ventricle. This study is based on six cases, one with..

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Since Kirklin described the first successful correction of double-outlet right ventricle (DORV), surgical repair has been extended to more complex forms of the malformation . In 1972, Lev and Bharati introduced..

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Double-outlet left ventricle (DOLV) is a rare congenital cardiac malformation in which both great arteries originate entirely or predominantly from the morphologic left ventricle. DOLV occurs most commonly in the..

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Double outlet right ventricle (DORV) is a rare congenital heart defect, meaning it’s a condition a baby is born with. In DORV, the pulmonary artery and the aorta — the..

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Double outlet right ventricle (DORV) is a . There is a malformation of the fetus heart in the womb leading to the right ventricle that has the two major arteries, namely..

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Double inlet left ventricle (DILV) is a heart defect that is present from birth (congenital). It affects the valves and chambers of the heart. Babies born with this condition have..

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Double inlet left ventricle (DILV) is a form of functionally univentricular heart where both the left and the right atrium are connected to the morphologically left ventricle. Usually, the morphologically..

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Double-chambered right ventricle (DCRV) was first described in 1858 by TB Peacock, but it is now understood to be a form of congenital heart disease wherein there is a mid-cavitary..

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Introduction Double aortic arch is the most common type of vascular ring malformation. It involves the complete encirclement and compression of the trachea and/or esophagus by the aortic arch, its..

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A heart with a criss-cross atrioventricular (AV) connection is a cardiopathy in which the ventricles are positioned contralaterally to the atria to which they are connected; the ventricular inflow tracts..

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A heart with a criss-cross atrioventricular (AV) connection is a cardiopathy in which the ventricles are positioned contralaterally to the atria to which they are connected; the ventricular inflow tracts..

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A heart with a criss-cross atrioventricular (AV) connection is a cardiopathy in which the ventricles are positioned contralaterally to the atria to which they are connected; the ventricular inflow tracts..

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A heart with a criss-cross atrioventricular (AV) connection is a cardiopathy in which the ventricles are positioned contralaterally to the atria to which they are connected; the ventricular inflow tracts..

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Dextroposition of the : The heart is displaced to the right (from its usual location in the left chest). There is no anatomic alteration in the heart itself, just in its location...

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Dextrocardia is a rare congenital disorder in which the heart resides on the right side of the thoracic cavity. It is often associated with other development anomalies and, in most..

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Unroofed coronary sinus syndrome (URCS) is a rare cardiac anomaly in which a communication occurs between the coronary sinus and the left atrium as a result of the partial or..

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Coronary artery fistulas (CAFs) are abnormal communications of coronary arteries whereby venous circuits bypass the normal capillaries within the myocardium. CAFs are rare, and most affected patients are asymptomatic. However,..

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Congenitally corrected transposition of the great arteries (CCTGA) is a rare heart defect in which the heart’s lower half is reversed. It is also called L-TGA. It is different from..

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Congenitally corrected transposition of the great arteries (CCTGA) is a rare congenital heart lesion with varied morphological presentation and can often by asymptomatic. A failing systemic right ventricle (RV) or..

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Congenitally corrected transposition of the great arteries (CCTGA) is a rare congenital heart lesion with varied morphological presentation and can often by asymptomatic. A failing systemic right ventricle (RV) or..

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Congenitally corrected transposition of the great arteries (CCTGA) is a rare congenital cardiac anomaly defined by atrio-ventricular and ventriculo-arterial discordance. This malformation makes up less than 1% of congenital heart defects...

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Congenitally corrected transposition of the great arteries (CCTGA) is a rare congenital cardiac anomaly defined by atrio-ventricular and ventriculo-arterial discordance. This malformation makes up less than 1% of congenital heart defects...

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Congenitally corrected transposition of the great arteries (CCTGA) is a rare congenital cardiac anomaly defined by atrio-ventricular and ventriculo-arterial discordance. This malformation makes up less than 1% of congenital heart defects...