动脉导管未闭(patent ductus arteriosus,PDA) 法洛四联症(tetralogy of Fallot,TOF) 房间隔缺损(atrial septal defect,ASD) 房间隔部位出现先天性缺损,造成左右心房间直接交通及血液分流的疾病称为房间隔缺损 心房水平左向右分流 右心血流量增加→右心系统扩大;...
Adults with congenital heart diseaseHeart failureTetralogy of FallotPulmonary regurgitationThe number of rTOF patients who survive into adulthood is steadily rising, with currently more than 90% reaching the third decade of life. However, rTOF patients are not cured, but rather have a lifelong ...
于胸骨旁大动脉短轴,分流束呈现以红色为主的五彩血流,起自降主动脉,经动脉导管进入肺动脉,沿主肺动脉外侧上升。 图 动脉导管未闭分流束由胸主动脉进入肺动脉 DTA:降主动脉胸段 PDA:动脉导管未闭 四.法乐氏四联症(Tetralogy of Fallot) 超声心动图表现...
There are many kinds of congenital heart diseases, which can be divided into patent ductus arteriosus, atrial septal defect, ventricular septal defect, tetralogy of Fallot, transposition of great arteries, pulmonary artery stenosis and aortic coarctation.[risk factors]1. It is related to the intraute...
Though the performances were generally good for most of the major CHD subtypes (see Table 1; especially for the tetralogy of fallot, atrioventricular septal defect, and double-outlet right ventricle), we also noticed that the detection sensitivity scores for some CHD subtypes (e.g., ASD and PD...
and NT-proBNP and Troponin T levels were assessed. The cardiac diagnoses were grouped into six CHD primary disease groups, namely, ASD, ventricular septal defect (VSD), complete atrioventricular septal defect (cAVSD), tetralogy of Fallot (ToF), TGA, and hypoplastic left heart syndrome (HLHS)/...
Congenital Heart Disease in Adults Atrial Septal Defect Ventricular Septal Defect Patent Ductus Arteriosus Aortic Stenosis Pulmonary Stenosis Parachute Mitral Valve Coronary Artery Fistula Anomalies of the Great Veins Tetralogy of Fallot Ebstein's Anomaly ...
(Figure 1). Advances in imaging technology have led to improved diagnostic precision.7Various constellations of multiple defects can be found together, and can result in more complex CHD, of which tetralogy of Fallot (TOF) is the most common form (Figure 1).11,12CHD may occur in apparent ...
Deletions within chromosome 22q11 in familial congenital heart disease. Lancet. 1992;340:573-5. Article PubMed CAS Google Scholar Trainer AH, Morrison N, Dunlop A, Wilson N, Tolmie J. Chromosome 22q11 microdeletions in tetralogy of Fallot. Arch Dis Child. 1996;74:62-3. Article PubMed ...