Adult Nigerian With Untreated Tetralogy Of Fallot- A Case Report

10.5580/2a62 ◽  
2012 ◽  
Vol 10 (2) ◽  
Author(s):  
Arindam Roy ◽  
Praveen Chavali ◽  
Shaikh Mohammed Husain ◽  
Neelam Bipinchandra Desai ◽  
Jinaga Nageswar Rao

2019 ◽  
Vol 5 (1) ◽  
Author(s):  
Ayano Teshigawara ◽  
Shinichi Nishibe ◽  
Saori Horie ◽  
Masako Hakone ◽  
Yoshihiro Yamaji ◽  
...  

2020 ◽  
Vol 30 (12) ◽  
pp. 1954-1956
Author(s):  
Harapriya Balasubramanian ◽  
Ragavan Munisamy ◽  
Robert Coelho

AbstractParagangliomas occurring with cyanotic heart disease is a known association. We present a case of an active paraganglioma in a child with unoperated Tetralogy of Fallot, which posed a management challenge considering the pathophysiology of both these conditions.


2011 ◽  
Vol 33 (1) ◽  
pp. 150-154
Author(s):  
Lowell H. Frank ◽  
T. K. Susheel Kumar ◽  
Richard A. Jonas ◽  
Mary T. Donofrio

2020 ◽  
Vol 5 (2) ◽  
pp. 1-7
Author(s):  
Patrycja Tesmer ◽  
Katarzyna Wróblewska-Seniuk ◽  
Jan Mazela ◽  
Jarosław Szydłowski

Congenital laryngeal stenosis is a rare and unusual anomaly that usually presents in the first minutes after delivery as severe life-threatening respiratory distress. It may exist as an isolated entity or in association with other congenital malformations, in particular cardiac anomalies. In this paper, we present the case of an infant with prenatal suspicion of tetralogy of Fallot. Immediately after delivery, the patient required intubation, which proved difficult. He was eventually diagnosed with laryngeal stenosis requiring laryngological treatment.


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