Imperforate anus, malrotation, and Hirschsprung's disease with double zonal aganglionosis: an extremely rare combination

2008 ◽  
Vol 43 (1) ◽  
pp. 222-226 ◽  
Author(s):  
Takehito Oshio
1995 ◽  
Vol 5 (03) ◽  
pp. 187-189 ◽  
Author(s):  
D. Poenaru ◽  
J. Uroz-Tristán ◽  
Suzanne Leclerc ◽  
S. Murphy ◽  
A. Bensoussan

1972 ◽  
Vol 39 (9) ◽  
pp. 297-299
Author(s):  
S. K. Bandi ◽  
J. Radhakrishnan ◽  
V. K. Agrawal

1985 ◽  
Vol 20 (3) ◽  
pp. 271-273 ◽  
Author(s):  
Yoshiteru Takada ◽  
Koji Aoyama ◽  
Takafumi Goto ◽  
Shigeru Mori

PEDIATRICS ◽  
1977 ◽  
Vol 59 (3) ◽  
pp. 469-472
Author(s):  
Diane E. Cooney ◽  
Jay L. Grosfeld

Colostomy in infancy and childhood is usually performed for benign disease and is of a temporary nature. The colostomy often may be functional for 12 to 18 months, however, and therefore requires skilled care by the patient and/or his parents. The purpose of this report is to describe a combined inpatient-outpatient program of colostomy care that has resulted in improved management of infants and children with colostomies. The physician, parent, nurse, and enterostomal therapist are all intimately involved in the program. It is further intended to acquaint the pediatric physician with complicating factors related to the procedure. Colostomies in children are frequently performed to relieve colonic obstructions resulting from congenital anomalies such as Hirschsprung's disease, colon atresia, and imperforate anus, and occasionally for pelvic and perineal tumors, Crohn's disease of the colon, and instances of rectal perforation.1,2


2001 ◽  
Vol 36 (4) ◽  
pp. 638-640 ◽  
Author(s):  
Ronaldo Hipolito ◽  
Michael Haight ◽  
Jeffrey Dubois ◽  
Jay Milstein ◽  
Boyd Goetzman

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