FEATURES OF INTENSIVE CARE OF CONGENITAL HEART MALFORMATIONS IN NEWBORNS

2020 ◽  
Vol 99 (3) ◽  
pp. 200-207
Author(s):  
D.O. Ivanov ◽  
◽  
K.V. Pshenisnov ◽  
Y.S. Aleksandrovich ◽  
◽  
...  
1981 ◽  
Vol 137 (4) ◽  
pp. 673-681 ◽  
Author(s):  
JG Arciniegas ◽  
B Soto ◽  
HC Coghlan ◽  
LM Bargeron

PEDIATRICS ◽  
1982 ◽  
Vol 70 (2) ◽  
pp. 328-328
Author(s):  
Louis E. Bartoshesky ◽  
Hermine Pashayan

We would agree with both writers that there were certain features of the child described in our report that were not typical of the so-called fetal hydantoin syndrome, particularly the birth weight. It is certainly true that single case reports do nothing more than suggest possible associations between malformations and in utero exposure, but much information has been accumulated associating clefts and congenital heart malformations with phenytoin. The baby described had a normal male karyotype. Attempts were made to do karyotyping on tissue obtained at autopsy but were unsuccessful.


Circulation ◽  
1975 ◽  
Vol 52 (5) ◽  
pp. 926-932 ◽  
Author(s):  
B J Maron ◽  
J E Edwards ◽  
V J Ferrans ◽  
C E Clark ◽  
E A Lebowitz ◽  
...  

1998 ◽  
Vol 8 (2) ◽  
pp. 265-270 ◽  
Author(s):  
Siew Yen Ho ◽  
Michael A. Gatzoulis ◽  
Mary Sheppard

AbstractAnomalous origin of a coronary artery is occasionally associated with other congenital heart malformations. Presence of the anomalous artery can then complicate surgical repair. We report an unusually complex arrangement in a patient who died 16 hours following complete surgical repair despite appropriate management.


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