Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Interrupted aortic arch type B"'
Autor:
Elizabeth Goldmuntz
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184:64-72
The 22q11.2 deletion syndrome has an estimated prevalence of 1 in 4-6,000 livebirths. The phenotype varies widely; the most common features include: facial dysmorphia, hypocalcemia, palate and speech disorders, feeding and gastrointestinal disorders,
Publikováno v:
JACC: Cardiovascular Interventions. 10:e163-e166
An asymptomatic 34-year-old woman with DiGeorge syndrome and interrupted aortic arch type B presented for care. She had undergone neonatal palliation with a 6-mm interposition graft followed by 16-mm extra-anatomic ascending to descending aortic jump
Publikováno v:
Journal of Cardiovascular Computed Tomography. 14:e73-e74
Publikováno v:
Annals of Pediatric Cardiology
Annals of Pediatric Cardiology, Vol 11, Iss 1, Pp 83-85 (2018)
Annals of Pediatric Cardiology, Vol 11, Iss 1, Pp 83-85 (2018)
An adolescent patient with a previous history of surgical repair for interrupted aortic arch type B presented with an asymptomatic, saccular pseudoaneurysm of the proximal, common left carotid artery, identified on a follow-up magnetic resonance angi
Publikováno v:
The Multimedia Manual for Cardio-Thoracic Surgery.
In this video tutorial, we present our surgical technique for single-stage complete repair of an interrupted aortic arch with ventricular septal defect. The key operative steps, which include dual cannulation, the arch repair, and the intra-cardiac r
Publikováno v:
Cardiology in the Young. 27:1229-1231
A 15-day-old premature patient with ventricular septal defect and interrupted aortic arch type B underwent “hybrid” initial treatment consisting of bilateral pulmonary artery banding followed by stenting of the ductus arteriosus. A pre-registered
Publikováno v:
Journal of the Saudi Heart Association, Vol 30, Iss 4, Pp 362-(2018)
Introduction The goal of this study is to describe (1) different types of isolation of arch branches and (2) to show the importance of careful evaluation of arch morphology using imaging tools such as echocardiography, cardiac computerized tomography
Publikováno v:
Interactive CardioVascular and Thoracic Surgery. 29:159-160
Aortic atresia with interrupted aortic arch is a rare anatomical and physiological combination. Survival is possible if there is blood flow in the ascending aorta supplying the coronary circulation from coexisting malformations. We present a newborn
Autor:
M.R. Noolu
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 54:290-290
Publikováno v:
Cardiology in the Young. 24:559-562
Adequate arch augmentation for interrupted aortic arch repair is quite important to avoid post-operative recoarctation and bronchial compression. We describe here two successful cases of aortic arch reconstruction using autologous materials such as a