Imperforate Anus, Malrotation and Hirschsprung's Disease: A Rare Association

1995 ◽  
Vol 5 (03) ◽  
pp. 187-189 ◽  
Author(s):  
D. Poenaru ◽  
J. Uroz-Tristán ◽  
Suzanne Leclerc ◽  
S. Murphy ◽  
A. Bensoussan
Keyword(s):  
Imperforate Anus ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease ◽  
Rare Association

Rare association of malrotation, imperforate anus and Hirschsprung's disease in an infant

2010 ◽  
Vol 52 (1) ◽  
pp. e9-e10 ◽  
Author(s):  
Chih-Cheng Luo ◽  
Yung-Ching Ming ◽  
Shih-Ming Chu ◽  
Hsun-Chin Chao
Keyword(s):  
Imperforate Anus ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease ◽  
Rare Association

Hirschsprung’s disease associated with imperforate anus

1972 ◽  
Vol 39 (9) ◽  
pp. 297-299
Author(s):  
S. K. Bandi ◽  
J. Radhakrishnan ◽  
V. K. Agrawal
Keyword(s):  
Imperforate Anus ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease

Hirschsprung's disease and asymptomatic malrotation: a rare association

1986 ◽  
Vol 16 (3) ◽  
pp. 250-251 ◽  
Author(s):  
O. Tamburrini ◽  
A. Bartolomeo-De Iuri ◽  
P. Palescandolo ◽  
A. Marte ◽  
G. Amici
Keyword(s):  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease ◽  
Rare Association

The association of imperforate anus and Hirschsprung's disease in siblings

1985 ◽  
Vol 20 (3) ◽  
pp. 271-273 ◽  
Author(s):  
Yoshiteru Takada ◽  
Koji Aoyama ◽  
Takafumi Goto ◽  
Shigeru Mori
Keyword(s):  
Imperforate Anus ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease

scholarly journals A Rare Co-occurrence of Intestinal Malrotation and Hirschsprung's Disease in a Neonate with 13q21.31q33.1 Interstitial Deletion Including the EDNRB Gene

2019 ◽  
Vol 08 (03) ◽  
pp. 142-146
Author(s):  
Trassanee Chatmethakul ◽  
Rozaleen Phaltas ◽  
Gwen Minzes ◽  
Jose Martinez ◽  
Ramachandra Bhat
Keyword(s):  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease ◽  
Interstitial Deletion ◽  
Intestinal Malrotation ◽  
Deletion Syndrome ◽  
Gastrointestinal Complications ◽  
Dysmorphic Features ◽  
Rare Association ◽  
Ednrb Gene ◽  
Male Neonate

AbstractWe report a rare co-occurrence of intestinal malrotation and Hirschsprung's disease (HSCR) in a male neonate with a large 38.8 Mb interstitial deletion of chromosome 13 extending from q21.31 to q33.1 including the EDNRB gene, who presented with craniofacial dysmorphic features and central nervous system malformations. The loss of EDNRB gene in addition to bilateral hearing loss and HSCR suggested an additional diagnosis of Waardenburg–Shah's syndrome. This case highlights the fact that prior knowledge of this rare association in infants with 13q deletion syndrome would enable early diagnosis and prompt interventions to prevent gastrointestinal complications.

Care of the Child With a Colostomy

PEDIATRICS ◽  
1977 ◽  
Vol 59 (3) ◽  
pp. 469-472
Author(s):  
Diane E. Cooney ◽  
Jay L. Grosfeld
Keyword(s):  
Imperforate Anus ◽  
Congenital Anomalies ◽  
Hirschsprung's Disease ◽  
Hirschsprung’S Disease ◽  
Benign Disease ◽  
Infants And Children ◽  
Rectal Perforation ◽  
Outpatient Program ◽  
Infancy And Childhood ◽  
Complicating Factors

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

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