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  Vol. 106 No. 1, January 1973 TABLE OF CONTENTS
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Congenital Pyloric Atresia in Siblings

Kim-Leong Tan, MB, BS, MRCPEd, D[ill]H; James J. Murugasu, MB, BS, FRACS

AMA Arch Surg. 1973;106(1):100-102.


Abstract

Congenital pyloric atresia is a very rare condition and, to our knowledge, has never been described in siblings. Two siblings (a male and a female) are described; the first sibling died from peritonitis, after operation to close gastric perforation. In the other sibling, the diagnosis was made by gastric aspiration of the last feeding just prior to the next, and gastroduodenostomy was successful. The possibility is raised of this being a genetically determined condition.



Author Affiliations

Singapore

From the Department of Pediatrics, University of Singapore.


Footnotes

Accepted for publication July 7, 1972.

Reprint requests to Department of Pediatrics, Faculty of Medicine, University of Singapore, Sepoy Lines, College Road, Singapore, 3 (Dr. Tan).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Familial Pyloric Atresia
SZALAY
Arch Pediatr Adolesc Med 1979;133:221-221.
ABSTRACT  

Pyloric Atresia
Konvolinka and Steward
Arch Pediatr Adolesc Med 1978;132:903-905.
ABSTRACT  

Congenital Pyloric Atresia
SZALAY
Arch Surg 1974;108:248-248.
ABSTRACT  

Congenital Pyloric Atresia in Siblings
KERAMIDAS
Arch Surg 1974;108:123-123.
ABSTRACT  





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