Age at operationPreoperative diagnosisOperationPostoperative courseSurvival 5 wk Bilateral pulmonary venous stenosis plus VSD Resection of bilateral pulmonary vein stenosis plus suture of VSD Died in operating room Died d 0 7 wk Hypoplastic LV plus hypoplastic mitral valve (MS) plus ASD plus Down syndr...
Background/aim: We aim to show pelvic lymphocele (PL) rates in patients who were operated for endometrial cancer (EC) and underwent systematic paraaortic bilateral pelvic lymph node dissection (PABPLND) with advanced bipolar vessel sealing device (ABVSD) Materials and method...
Fetal echo is short for fetal echocardiogram, an ultrasound test doctors use to look forcongenital heart disease(CHD). This disease affects around 1% of births each year and encompasses a wide range of heart issues. The most common CHD diagnosis is calledventricular septal defect(VSD). Understand...
Should coronary artery bypass grafting be performed at the same time as repair of a post-infarct ventricular septal defect? OBJECTIVE: The value of coronary artery bypass grafting (CABG) at the time of repair of a post-infarct ventricular septal defect (VSD) remains controversia... Dalrymple-...
For example, histologically confirmed absence of portal vein in the liver is mandatory in the diagnosis. Abernethy type II was previously misclassified as CAPV[21]. Kerlan et al[96] reported a case similar to CAPV, but surgery for closing the fistula between portal vein and inferior cava, ...
(VSD), which offered us with rich experiences on MTCST (7,9). Herein, we will demonstrate the application of MTCST for patients undergoing MVR and establish the safety and feasibility of this technique based on a relatively large patient cohort. In addition, the in-hospital results and ...
If no mutations are found additional NPHP genes should be screened depending on phenotype and a differential diagnosis of MCKD, ARPKD and BBS should be considered. Nephronophthisis and disease associations Many disorders have been described in which NPHP is a clinical feature. Such multisystem ...
Many of our patients were initially eval- uated for Fragile X, DiGeorge, Down, or Prader-Willi syn- dromes, and the diagnosis of SMS was only considered much later. Although we conclude that haploinsufficiency of RAI1 is responsible for most of the SMS features, the involvement of other ...
SHORCAL SHORE SHORECAL SHORLAC SHOROC SHORSTAMPS SHORT Short Time Fourier Transform SHORTZ SHOT SHOTS SHOUT SHOVE SHOVER SHOW SHOWL SHOWW2 SHOX SHP SHP-1 SHP2 SHPA SHPAG SHPB SHPC SHPCA SHPCC SHPCH SHPCS SHPD SHPDA SHPDO SHPE ▼...
the syndrome, cases that are found by chance are often initially suspected due to the presence of the characteristic heart defect involving the outflow tract, and are then screened for 22q11.2 deletion by fluorescence in situ hybridization (FISH) or other methods for a diagnosis of the syndrome...