Hirschsprung disease (HSCR) is the leading cause of neonatal functional intestinal
obstruction. It is a rare congenital disease with an incidence of one in 3,500–5,000 live …

Background Congenital anomalies are a leading cause of morbidity and mortality
worldwide. We aimed to review the common surgically correctable congenital anomalies …

Introduction Published studies based on Krickenbeck classification of anorectal
malformations (ARMs) are still insufficient to assess the global as well as regional relative …

Purpose Hirschsprung's disease (HD) is a rare occurrence in premature infants, and the
exact prevalence varying across studies. Thus, we conducted this study to determine the …

While the development from child to adult spans the first 8000 days (or 21 years) of life,
much of the focus in global child health has been on the first 1000 days of life (between …

Hirschsprung's disease (HSCR) is known to occur in families. In affected families, the
reported overall incidence of HSCR is 7.6%, increasing to 15–21% in total colonic …

HSCR, auch Aganglionose oder kongenitales Megakolon, bezeichnet eine angeborene
Erkrankung, die durch eine fehlende Innervation des Darms charakterisiert ist …

Objectives: This article evaluates current data in literature on the definition, outcomes, and
current management strategies for patients with Hirschsprung's disease (HD). Methods …

Background: Hirschsprung's disease is a major cause of functional intestinal obstruction,
mainly affecting the distal region of the large intestine. Risk factors for this disease include a …

Total colonic aganglionosis occurring together with malrotation is a rare occurrence and
may pose diagnostic and management dilemmas for the pediatric surgeon. We report the …