Results 121 to 130 of about 5,922 (184)

The burden of delayed diagnosis in Hirschsprung disease: insights from a Paediatric Colorectal Centre in South Africa. [PDF]

open access: yesBMC Pediatr
Trovalusci E   +5 more
europepmc   +1 more source

Impaired Fertility and Sexual Function in Women With Hirschsprung Disease: Results From an International Multi-Centre Cross-Sectional Study. [PDF]

open access: yesBJOG
Davidson JR   +10 more
europepmc   +1 more source

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

Hirschsprung disease

Seminars in Pediatric Surgery, 2008
Hirschsprung disease is a relatively common condition managed by pediatric surgeons. Significant advances have been made in understanding its etiologies in the last decade, especially with the explosion of molecular genetic techniques and early diagnosis. The surgical management has progressed from a two- or three-stage procedure to a primary operation.
Ramanath N Haricharan, Keith E Georgeson
exaly   +3 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

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