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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
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Hirschsprung's disease (HSCR) is characterized by absence of the enteric nervous system in a variable portion of the distal gut. Affected infants usually present in the days after birth with bowel obstruction.
GarciaBarcelo, M, Kenny, SE, Tam, PKH
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Early presentation of Hirschsprung’s disease with initial meconium passage: A diagnostic challenge [PDF]
Hirschsprung’s disease is a congenital condition characterized by an absence of enteric ganglionic cells. In this paper, we report a case of an 8-day-old male infant presenting with a history of constipation and progressive abdominal distension. Meconium
Tuba Chaudry, Susan Flesher
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Advance in susceptibility genes and epigenetic regulation in Hirschsprung's disease [PDF]
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
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PurposeRadical surgery is the most effective treatment for Hirschsprung's disease. However, some children still have symptoms of intestinal dysfunction such as constipation, abdominal distension, and recurrent enterocolitis after operation.
Li Tian +17 more
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The Classification and Surgical Treatments in Adult Hirschsprung’s Disease: A Retrospective Study
PurposeTo explore the treatments and short-term effects of different types of adult Hirschsprung’s disease.Methods89 patients treated in Shanghai Changhai Hospital were retrospectively analyzed.
Shengzhe Ma +9 more
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Enteric Neurospheres Are Not Specific to Neural Crest Cultures: Implications for Neural Stem Cell Therapies [PDF]
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work ...
A Barlow +61 more
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Adult Hirschsprung’s disease presenting as chronic constipation: a case report
Background Hirschsprung’s disease is a congenital disorder identified by the absence of ganglion cells at the Meissner’s plexus of the submucosa and Auerbach’s plexus of the muscularis. This disease can be found in approximately 1 in 5000 live births. It
Theresia Monica Rahardjo +6 more
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Hirschsprung's Disease - Review of Clinical Features, Diagnosis and Treatment
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
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Familial Experience With Hirschsprung's Disease Improves the Patient's Ability to Cope
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
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