scholarly journals Interstitial deletion of chromosome 1 (1p21.1p12) in an infant with congenital diaphragmatic hernia, hydrops fetalis, and interrupted aortic arch

2017 ◽  
Vol 5 (2) ◽  
pp. 164-169 ◽  
Author(s):  
Masitah Ibrahim ◽  
Matthew Hunter ◽  
Lucy Gugasyan ◽  
Yuen Chan ◽  
Atul Malhotra ◽  
...  
2017 ◽  
Vol 27 (5) ◽  
pp. 1018-1021 ◽  
Author(s):  
Ziyad M. Binsalamah ◽  
Peter Chen ◽  
Emmett D. McKenzie

AbstractPersistence of the fifth aortic arch is a very rare anomaly, but is clinically relevant when it is associated with coarctation. We report a case of a neonate with type A interrupted aortic arch and severe coarctation of a persistent fifth aortic arch, which was discovered after repair of a left congenital diaphragmatic hernia. The combination of anomalies was discovered intra-operatively following left thoracotomy, and was treated with aortic arch advancement. The postoperative course was uneventful.


2019 ◽  
Vol 29 (10) ◽  
pp. 1307-1309 ◽  
Author(s):  
Lijun Yang ◽  
Lifen Ye ◽  
Ru Lin

AbstractWe report a neonatal case of the use of alteplase for the lysis of a large aortic arch thrombus formed during extracorporeal membrane oxygenation support. Alteplase (0.1–0.15 mg/kg/hour) was infused for thrombolysis, and meanwhile, unfractionated heparin was administrated at 5–10 U/kg/hour for the anticoagulation purpose. Alteplase was successfully administered to this neonate after the repair of congenital diaphragmatic hernia on extracorporeal membrane oxygenation, and the patient survived without apparent catastrophic long-term complications. It is reasonable to consider alteplase therapy during extracorporeal membrane oxygenation support in this setting.


2011 ◽  
Vol 32 (8) ◽  
pp. 1207-1208 ◽  
Author(s):  
Poonam P. Thankavel ◽  
Claudio Ramaciotti ◽  
Matthew S. Lemler

2014 ◽  
Vol 2 (1) ◽  
pp. 15-19
Author(s):  
Ryo Ishii ◽  
Noboru Inamura ◽  
Akio Kubota ◽  
Futoshi Kayatani ◽  
Mayumi Shimada ◽  
...  

2014 ◽  
Vol 24 (4) ◽  
pp. 725-726
Author(s):  
Joanne S. Chiu ◽  
Julie Glickstein ◽  
Amee Shah

AbstractCongenital heart disease is associated with congenital diaphragmatic hernia, but diagnosis by echocardiography can be difficult. We present the unusual case of a patient with a double aortic arch and congenital diaphragmatic hernia diagnosed using cardiac magnetic resonance imaging.


2002 ◽  
Vol 41 (5) ◽  
pp. 441-447
Author(s):  
Tröbs R.-B. ◽  
Wild L. ◽  
Klöppel R. ◽  
Bennek J.

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