Hirschsprung disease (HD) is a congenital condition that affects intestinal function due to the
absence of ganglion cells in the myenteric and submucosal plexus of the colon. This …

Hirschsprung's disease is a congenital disorder that affects the motility of the colon. It is
caused by the absence of ganglion cells in the large intestinal plexuses. Although …

Introduction: The primary aim of surgical procedures for Hirschsprung's disease is to
establish proper bowel movement without fecal incontinence, constipation and entrocolitis …

Review on RET gene and protein, a membrane tyrosine kinase receptor involved in various
cancers, including papillary thyroid carcinoma, lung cancer, breast cancer, colorectal …

Background: Hirschsprung disease (HSCR) is a developmental disorder characterized by
the absence of ganglion cells in the gastrointestinal tract, which consequences in intestinal …