Results 11 to 20 of about 3,329 (135)

Hirschsprung's Disease - Review of Clinical Features, Diagnosis and Treatment

open access: yesJournal of Education, Health and Sport, 2023
Introduction and purpose: Hirschsprung's disease, also known as congenital aganglionic megacolon, is a rare congenital disorder that affects the large intestine.
Rafał Tkaczyk   +9 more
doaj   +1 more source

Hirschsprung’s Disease—Recent Understanding of Embryonic Aspects, Etiopathogenesis and Future Treatment Avenues

open access: yesMedicina, 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

Maternal use of selective serotonin reuptake inhibitors during pregnancy is associated with Hirschsprung’s disease in newborns – a nationwide cohort study

open access: yesOrphanet 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   +1 more source

Delayed diagnosis of Hirschsprung's disease associated with colonic atresia and multiple anomalies: Report of a case and review of the literature

open access: yesJournal 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

open access: yesJournal 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

Predictability of 48-h delayed retention of contrast in barium enema in cases of chronic constipation

open access: yesAfrican Journal of Paediatric Surgery, 2020
Introduction: Diagnosis of Hirschsprung's disease depends on rectal biopsy. This study was designed to find an alternate diagnostic modality to exclude Hirschsprung's disease.
Nitin Sharma   +5 more
doaj   +1 more source

Validity of Barium Enema as Hirschsprung’s Disease Diagnostic Tools for Infant in Sanglah Hospital Denpasar

open access: yesJBN (Jurnal Bedah Nasional), 2021
Aim: To determine the validity (sensitivity, specificity, likelihood ratio) of barium enema as Hirschsprung's disease diagnostic tool in infants. Methods: This study was a diagnostic test of barium enema compared with postoperative histopathology ...
I Made Darmajaya, I Ketut Subhawa
doaj   +1 more source

A case of Hirschsprung's disease underwent surgery in adulthood

open access: yesJournal of Pediatric Surgery Case Reports, 2016
Adult Hirschsprung's disease is a rare motor disorder of the gut that is frequently misdiagnosed as refractory constipation. We describe a 30-year-old patient with adult Hirschsprung's disease with a history of chronic constipation requiring daily enema.
Richi Nakatake   +7 more
doaj   +1 more source

Neuroimmune regulation in Hirschsprung’s disease associated enterocolitis

open access: yesFrontiers 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   +1 more source

Congenital intestinal hypoganglionosis: A radiologic mimic of Hirschsprung's disease

open access: yesRadiology Case Reports, 2019
Intestinal hypoganglionosis or isolated hypoganglionosis is a rare entity with a clinical and radiologic presentation that can mimic Hirschsprung's disease in the neonatal period.
Gayathri Sreedher, MD   +4 more
doaj   +1 more source

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