scholarly journals Pentalogy of Cantrell with a double-outlet right ventricle: Prenatal Diagnosis, Delivery and Immediate Postnatal Surgical Repair / Pentalogia de Cantrell com um ventrículo direito de saída dupla: Diagnóstico Pré-Natal, Parto e Reparação Cirúrgica Pós-Natal Imediata

2021 ◽  
Vol 7 (10) ◽  
pp. 96848-96857
Author(s):  
Camilla Azevedo Bringel ◽  
Renata de Medeiros Wanderley Gadelha ◽  
Carolina Lima Santos ◽  
Hélita Bezerra Freitas ◽  
Thiago Cavalcanti Vila Nova De Araújo ◽  
...  
2019 ◽  
Author(s):  
D. Wagner ◽  
C. Gall ◽  
A. Rüffer ◽  
A. Purbojo ◽  
S. Dittrich ◽  
...  

2007 ◽  
Vol 167 (1) ◽  
pp. 103-105 ◽  
Author(s):  
Junji Takaya ◽  
Naoyuki Kitamura ◽  
Kimiko Tsuji ◽  
Kentaro Watanabe ◽  
Yo Kinoshita ◽  
...  

2012 ◽  
Vol 28 (3) ◽  
pp. 196-201
Author(s):  
Tadashi Wada ◽  
Atsuyuki Watanabe ◽  
Yuji Koide ◽  
Kenzo Kagawa ◽  
Yoichiro Naito ◽  
...  

2017 ◽  
Vol 27 (5) ◽  
pp. 996-999 ◽  
Author(s):  
Gaku Izumi ◽  
Hisashi Yokoshiki ◽  
Atsuhito Takeda

AbstractCatheter ablation of ventricular tachycardia is often difficult in patients after surgery for CHD. In patients with a ventricular septal defect patch, it is necessary to decide which ventricular side is appropriate for catheter ablation. In this article, we report a case of successful point catheter ablation of re-entrant ventricular tachycardia. Identification of the ventricular septal defect patch using intra-cardiac echocardiography was useful.


2005 ◽  
Vol 33 (4) ◽  
pp. 197-200 ◽  
Author(s):  
Theera Tongsong ◽  
Rekwan Sittiwangkul ◽  
Chanane Wanapirak ◽  
Supatra Sirichotiyakul

2003 ◽  
Vol 11 (3) ◽  
pp. 115-117 ◽  
Author(s):  
Liezl Augusto ◽  
Yoshihide Chiba ◽  
Shiho Endo ◽  
Yuki Ishihara

2017 ◽  
Vol 6 (2) ◽  
pp. 32 ◽  
Author(s):  
Edward Araujo Júnior ◽  
Milene Carvalho Carrilho ◽  
Bruno Rodrigues Toneto ◽  
José Cicero Guilhen

Pentalogy of Cantrell (PC) is a congenital anomaly characterized by a defect in the lower sternum, anterior diaphragm, and anterior abdominal wall; ectopia cordis; and congenital heart disease. It is a very rare congenital anomaly and the prenatal diagnosis is possible in the beginning of second trimester of pregnancy using the conventional ultrasonography. The prognosis is poor with high rates of perinatal mortality. We present a case report of prenatal diagnosis of PC at 22 weeks and 3 days of gestation. We emphasize the prenatal care follow up in a tertiary reference center, the parental counseling, the planning of delivery, and the management of newborn by a multidisciplinary team, including the description of immediate postnatal surgical repair.


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