Hirschsprung's disease (HSCR) is a complex congenital disorder which, from a molecular
perspective, appears to result due to disruption of normal signalling during development of …

Purpose Down syndrome (DS) is the most frequent chromosomal abnormality associated
with Hirschsprung's disease (HD). It has often been suggested that this association results in …

Hirschsprung's disease (HD), congenital absence of ganglion cells, is considered
uncommon in preterm infants. The aim was to describe the frequency, presentation, and …

Background Hirschsprung disease is a neonatal discovery in almost all cases, and the
association of Hirschsprung disease in adults with symptomatic intestinal malrotation is …

The author describes an extremely rare case of coexistence with imperforate anus,
malrotation, and double zonal aganglionosis. A colostomy was performed on a 2-day-old …

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Hirschsprung's disease is a complex congenital disorder mostly of genetic origin, which from
a molecular perspective appears to result from disruption of normal signalling during …

Aim: Associated anomalies in neonates with congenital anomalies are important reasons of
mortality and morbidity in neonatal surgery units. Associated anomalies may be diagnosed …

Background Multiple etiologies exist for neonatal intestinal obstruction with similar
presenting symptoms. While single etiology is the most common cause, concomitant surgical …

Malrotation and Hirschsprung's disease (HSD) are rarely reported together. We report our
experience with three patients who presented during the neonatal period in whom the …