Hirschsprung disease (HSCR) is a rare congenital intestinal disease that occurs in 1 in
5,000 live births. HSCR is characterized by the absence of ganglion cells in the myenteric …

After operative intervention for Hirschsprung disease (HD) a child should thrive, be fecally
continent, and avoid recurrent episodes of abdominal distention and enterocolitis. This is …

Children with Hirschsprung disease have postoperative long-term sequelae in defecation
that contribute to morbidity and mortality and significantly impact their quality of life. Pediatric …

Robotic colorectal surgery allows adult and pediatric surgeons to overcome the technical
limitations of laparoscopic surgery. It also provides improved ergonomics in the field of …

Abstract Purpose of Review Ideally, after operative intervention, a child born with
Hirschsprung disease (HD) should thrive, achieve fecal continence, and avoid recurrent …

Background Hirschsprung's disease (HD) is a rare congenital disease that is characterised
by the absence of ganglion cells in the myenteric plexus starting in the distal bowel. This …

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 …

Objectives Abnormal motility of the residual colon has been reported in post‐pull‐through
Hirschsprung disease (PT‐HSCR) patients with persistent defecation problems. We …

Hirschsprung's disease (HD) is a congenital disorder, characterized by aganglionosis in the
distal part of the gastrointestinal tract. Despite complete surgical resection of the aganglionic …

Hirschsprung disease (HD) is a complex surgical and medical problem that appears to have
varied health and social outcomes with the age and neurodevelopmental state of patients. In …