Introduction Little is known about psychosocial and behavioral factors that impact the quality
of life of patient's with anorectal malformations (ARM) and Hirschsprung disease (HSCR) …

Abstract Objective Long-Segment Hirschsprung Disease (LSHD) differs clinically from short-
segment disease. This review article critically appraises current literature on the definition …

Abstract Background/Purpose The need for transitional care has gained increased focus in
the treatment of patients with congenital colorectal disorders. We aimed to acquire in-depth …

Background No systematic review and meta-analysis to date has examined multiple child
and parent-reported social and physical quality of life (QoL) in pediatric populations affected …

Hirschsprung disease (HSCR) and Paediatric Intestinal Pseudo-obstruction (PIPO) comprise
two of the most recognized and severe disorders of gastrointestinal (GI) motility. HSCR is a …

Anorectal malformation (ARM) and Hirschsprung's disease (HD) are the most common
congenital colorectal anomalies. Despite advances in surgical techniques and …

Objective: This multicentric study aimed to evaluate the quality of life (QOL) in children with
Hirschsprung's disease (HD). Methods: HD patients aged from 6 to 18 years and followed …

Anorectal malformations (ARM) and Hirschsprung disease (HD) are hindgut anomalies in
which the rectum is either abnormally located or abnormal in function, respectively …

Aims The purpose of this study was to assess bowel function and quality of life (QoL) in
patients with Hirschsprung's disease (HD) and identify patients who have 'failed'treatment …

Bowel dysfunction has been proven to be the most typical complication of long-segment
Hirschsprung disease (LSHD). Additionally, bowel dysfunction in preschool and early …