Algorithm for Surgical Treatment of Children with Hirschsprung’s Disease [PDF]
Galician Medical Journal, 2019 Hirschsprung’s disease requires surgical treatment. Depending on the form of aganglionosis and severity of pathology, open or minimally invasive, one-stage or multi-stage radical surgery may be used.
Oleh Kurtash
doaj +3 more sources
Neuroimmune regulation in Hirschsprung’s disease associated enterocolitis [PDF]
Frontiers in Immunology, 2023 Neuroimmune pathways are important part of the regulation of inflammatory response. Nerve cells regulate the functions of various immune cells through neurotransmitters, and then participate in the inflammatory immune response. Hirschsprung’s disease (HD)
Haosen Ji, Dengming Lai, Jinfa Tou
doaj +2 more sources
Maternal use of selective serotonin reuptake inhibitors during pregnancy is associated with Hirschsprung’s disease in newborns – a nationwide cohort study [PDF]
Orphanet Journal of Rare Diseases, 2017 Background Hirschsprung’s disease is a rare condition caused by congenital malformation of the gastrointestinal tract affecting 1:5000 children. Not much is known about risk factors for development of Hirschsprung’s disease.
Sebastian Werngreen Nielsen +4 more
doaj +2 more sources
Hirschsprung’s Disease in Patients of Advanced Age [PDF]
International Journal of Gerontology, 2012 Hirschsprung’s disease is a congenital motility disorder that is easily overlooked as a cause of chronic refractory constipation in adults. We present a case of Hirschsprung’s disease in a patient 70 years of age with a history of long-standing ...
Ina Vrints +5 more
doaj +2 more sources
STUDY OF OUTCOME AND COMPLICATIONS OF ANORECTAL MYECTOMY IN CHILDREN WITH ULTRASHORT SEGMENT HIRSCHSPRUNG’S DISEASE [PDF]
Acta Medica Iranica, 2006 The term ultra short is not clearly defined in ultrashort-segment Hirschsprung’s disease. The limited extent of the ultrashort-segment Hirschsprung’s disease allows for treatment with extended sphincteromyectomy.
J. Ahmadi +7 more
doaj +3 more sources
Comparing surface electroenterography measurements between patients suffering from Hirschsprung’s disease and controls: a feasibility study [PDF]
Scientific ReportsCurrent diagnostics in Hirschsprung’s disease are often challenging and invasive. This study aims to investigate whether surface electroenterography can non-invasively discern healthy subjects from subjects suffering from Hirschsprung’s disease.
Nick Rolleman +5 more
doaj +2 more sources
Familial Experience With Hirschsprung's Disease Improves the Patient's Ability to Cope
Frontiers in Pediatrics, 2022 IntroductionFamilial occurrence of Hirschsprung's disease may have a positive effect on patients' ability to cope with the disease. The aim was to compare long-term bowel function and generic quality of life between patients with familial and non ...
Sanne J. Verkuijl +13 more
doaj +1 more source
Medicina, 2020 Hirschsprung’s disease is a neurocristopathy, caused by defective migration, proliferation, differentiation and survival of neural crest cells, leading to gut aganglionosis. It usually manifests rapidly after birth, affecting 1 in 5000 live births around
Martin Klein, Ivan Varga
doaj +1 more source
Journal of Pediatric Surgery Case Reports, 2016 The co-occurrence of colonic atresia and Hirschsprung's disease is extremely rare and presents a diagnostic and therapeutic challenge. Although colonic atresia is usually recognized shortly after birth, the diagnosis of co-existent Hirschsprung's disease
Jinyoung Park
doaj +1 more source
A rare association of ileal atresia and total colonic Hirschsprung's disease
Journal of Pediatric Surgery Case Reports, 2022 Total colonic aganglionosis is the most rare form of Hirschsprung's disease and is defined as the absence of ganglion cells in both myenteric and submucosal plexus extending from the anus to at least the ileocecal valve. Intrauterine intussusceptions, on
Aida Daib +5 more
doaj +1 more source