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Hirschsprung disease

Nature Reviews Disease Primers, 2023
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 and submucosal plexuses of the intestine. Most patients present during the neonatal period with the first meconium passage delayed beyond 24 h, abdominal distension and ...
Louise Montalva   +9 more
openaire   +5 more sources

The Hirschsprungs patient who is soiling after what was considered a “successful” pull-through

open access: yesSeminars in Pediatric Surgery, 2012
After surgery for Hirschsprungs disease, most children thrive, have few if any episodes of abdominal distention and enterocolitis, and are fecally continent. However, there exists a small group of patients who do not do well.
Peña, Alberto   +2 more
exaly   +2 more sources

Hirschsprung Disease

Pediatrics In Review, 1995
In 1886, Harald Hirschsprung first described a disorder in newborns of severe constipation with dilatation and hypertrophy of the colon. No mechanical obstruction could be demonstrated, but there appeared to be an area of spasm that prevented the movement of lumen contents through the sigmoid or rectum. This disorder, termed Hirschsprung disease, later
C, Rudolph, L, Benaroch
openaire   +2 more sources

New method of transanal pull through operation in patients with hirschsprungs disease

open access: yesAfrican Journal of Paediatric Surgery
Hirschsprungs disease is an enteric nervous system dysfunction. Although, several types of pull through operations exist for this condition, each has its own pros and cons.
Saeed Gholamzadeh
exaly   +2 more sources

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