Results 1 to 10 of about 30,650 (133)
Redo Pull-through in Hirschsprungs Disease - A Meta-Analysis of Outcomes Based on type of Pull-through [PDF]
Journal of Indian Association of Pediatric SurgeonsPurpose: The meta-analysis investigates the effects of redo pull-through (PT) surgeries on bowel function outcomes in patients with rectosigmoid and long-segment Hirschsprung’s disease (HD) who have already undergone an initial PT. By comparing different
M. Srinivasa Rao +2 more
doaj +4 more sources
Botulinium toxin, as bridge to transanal pullthrough in neonate with Hirschsprungs disease [PDF]
Journal of Indian Association of Pediatric Surgeons, 2008 Aims and Objectives: The aim of this study is to find easier way of home care while obviating the colostomy before single stage pull through operation.
Hosseini SMV +3 more
doaj +2 more sources
The Clinical Impact of Delayed Management of Hirschsprungs Disease [PDF]
Zagazig University Medical Journal, 2022 Background: Hirschsprung's disease (HD) is a developmental disorder of the enteric nervous system that is characterized by the absence of ganglion cells in the myenteric and submucosal plexus from the anorectum for a variable colonic or intestinal ...
Ahmed Rozeik +3 more
doaj +1 more source
Gastroenterology Insights, 2023 Introduction: Congenital anomalies (CA’s) of most of the gastrointestinal tract have been linked causally with prenatal or community cannabis exposure. Therefore, we studied this relationship in Europe. Methods: CA data were from Eurocat.
Albert Stuart Reece, Gary Kenneth Hulse
doaj +1 more source
Stercoral ulcer after Hirschsprung's disease surgery
Clinical Case Reports, 2021 Constipation and stercoral ulcer are risk factors associated with Hirschsprung's disease (HD); long‐term follow‐up is, thus, essential. In postoperative HD associated with Down syndrome (DS) with intellectual disability, vigilant follow‐up is required to
Toshihiko Kakiuchi +5 more
doaj +1 more source
Anorectal malformation combined with Hirschsprung's disease: a case report
Frontiers in Pediatrics, 2023 Anorectal malformation (ARM) and Hirschsprungs disease (HSCR) are frequently associated with other congenital malformations, but rarely with one another.
Jiansen Fan +4 more
doaj +1 more source
Delayed presentation of preterm Hirschsprung's disease
Journal of Pediatric Surgery Case Reports, 2020 Hirschsprung's disease (HD) in a very low birth weight, preterm infant is a rare occurrence. We present a case of a baby born at 29 weeks gestation, who after stooling normally for several weeks, developed a large bowel obstruction on day of life (DOL ...
Henry P. Miller +2 more
doaj +1 more source
Fine mapping of the NRG1 Hirschsprung's disease locus. [PDF]
PLoS ONE, 2011 The primary pathology of Hirschsprung's disease (HSCR, colon aganglionosis) is the absence of ganglia in variable lengths of the hindgut, resulting in functional obstruction. HSCR is attributed to a failure of migration of the enteric ganglion precursors
Clara Sze-Man Tang +18 more
doaj +1 more source
Advance in susceptibility genes and epigenetic regulation in Hirschsprung's disease [PDF]
Jichu yixue yu linchuang, 2023 Hirschsprung's disease(HSCR)is a disease resulted from abnormal enteric nervous system development. The abnormal coding of related genes may affect the migration, proliferation, differentiation or survival of neural crest cells in digestive tract and ...
WANG Taiyao, ZHENG Lifei
doaj +1 more source
HIRSCHSPRUNG'S DISEASE − EARLY AND LATE COMPLICATIONS
Slovenska pediatrija, 2020 Hirschsprung’s disease is a congenital disruption of bowel motility, which occurs in approximately 1 / 5000 births. Timely recognition and treatment of the disease are of utmost importance in enabling the affected children to have good functional ...
Jože Maučec +2 more
doaj +1 more source