Αποτελέσματα Αναζήτησης
DOLV is a malformation in which the aorta and pulmonary artery arise predominantly or exclusively from the left ventricle. The classification of DOLV is based on the following criteria: Situs solitus (normal). Situs inversus. Situs ambiguous. Concordant or discordant alignment. Double inlet. Absent left or right atrioventricular connection.
14 Απρ 2018 · Double outlet left ventricle (DOLV) is an extremely rare congenital cardiac anomaly where both the aorta and pulmonary trunk arise from the anatomical left ventricle. It is usually classified as a conotruncal anomaly and is often associated with a ventricular septal defect with normal continuity between the aortic valve and anterior mitral valve .
Double outlet RV (DORV) is characterized by the origin of more than 50% of both the aorta and PA from the RV and is caused by abnormal spiraling of the truncus arteriosus and the arrest of membranous septal formation. It accounts for less than 1% of congenital heart defects and is seen in 0.08–0.16 per 1000 live births . There are four types ...
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 form of atrial situs solitus with atrioventricular (AV) concordance.
Double outlet left ventricle (DOLV) is a very rare anomaly characterized by the aortic (Ao) and pulmonary artery originating entirely or predominantly from the left ventricle. Dual outlet ventricles with compatible atrioventricular (AV) connections account for 1% of congenital heart diseases, and DOLV
12 Μαρ 2023 · Double outlet left ventricle, as the name suggests, describes origin of both great arteries from the morphologic left ventricle (Manner et al. 1997; Tchervenkov et al. 2000). More specifically, the whole of one great artery and at least half of the other must originate from the left ventricle (Stegmann et al. 1979 ).
30 Μαρ 2016 · Double outlet left ventricle (DOLV) is a rare congenital cardiac malformation in which both great arteries arise entirely or predominantly from the morphologic left ventricle. Dextroposition of the posterior great artery causes double outlet right ventricle, while levoposition of the anterior great artery causes DOLV.
