scholarly journals CONGENITAL ATRESIA OF ESOPHAGUS

1956 ◽  
Vol 32 (3) ◽  
pp. 332-346 ◽  
Author(s):  
George H. Humphreys ◽  
Bruce M. Hogg ◽  
Jose Ferrer
Keyword(s):  
1986 ◽  
Vol 94 (6) ◽  
pp. 574-577 ◽  
Author(s):  
Douglas E. Mattox ◽  
Ugo Fisch

Severe congenital atresia of the ear often requires—or indicates the need for—reconstructive surgery. We have developed a new technique for reconstruction of the external auditory canal. What follows is description of this technique and the results of its implementation.


PEDIATRICS ◽  
1969 ◽  
Vol 43 (1) ◽  
pp. 79-83
Author(s):  
Eric W. Fonkalsrud ◽  
Alfred A. deLorimier ◽  
Daniel M. Hays

A review is presented of 503 patients with congenital duodenal obstruction, compiled from 65 hospitals by the Surgical Section of the American Academy of Pediatrics. Four hundred eighty-seven patients underwent primary operative correction of the malformation with an overall early and late mortality rate of 36%. Complications from associated major congenital malformations were the leading cause of death. Many of these anomalies were potentially correctable had they been recognized and early treatment instituted. More than half of the infants with duodenal atresia had associated malformations. Thirty percent of the patients had Down's syndrome. End-to-side or side-to-side duodenoduodenostomy or jejunostomy are the most commonly used operative techniques for duodenal atresia. General anesthesia and tube gastrostomy are usually employed.


2018 ◽  
Vol 74 (6) ◽  
pp. 549-550
Author(s):  
Niraj Nirmal Pandey* ◽  
Mumun Sinha ◽  
Arun Sharma ◽  
Sanjeev Kumar

1948 ◽  
Vol 128 (6) ◽  
pp. 1173-1177 ◽  
Author(s):  
CHARLES B. RIPSTEIN ◽  
G. Gavin Miller

Author(s):  
André Ataíde ◽  
Marcela Oliveira ◽  
Yasser Jebahi ◽  
Tatiana Patruni ◽  
Talita Andreassa

1958 ◽  
Vol 15 (6) ◽  
pp. 688-694 ◽  
Author(s):  
Hal C. Holland ◽  
Wistar L. Graham
Keyword(s):  

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