Results 251 to 260 of about 9,333,061 (296)
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Variant Hirschsprung’s disease
Seminars in Pediatric Surgery, 2004Conditions that clinically resemble HD despite the presence of ganglion cells on suction rectal biopsy results, can be diagnosed by providing an adequate biopsy and employing a variety of histological techniques. Intestinal neuronal dysplasia is a distinct clinical entity that can be clearly proven histologically.
Prem, Puri, Udo, Rolle
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Neonatal Hirschsprung’s disease
The Indian Journal of Pediatrics, 2000Since the classic description of this disease by Harold Hirschsprung's. In 1886 just over a century ago, there has been a marked evolution in the diagnostic modalities, understanding of the pathophysiology, unraveling of genetic association and the treatment approach of this disease.
A, Lall, D K, Gupta, M, Bajpai
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Adult Segmental Hirschsprung Disease
Southern Medical Journal, 2009Hirschsprung disease (HD) is characterized by aganglionosis, which mainly occurs in the rectum and distal sigmoid colon. Typical HD is seldom diagnosed in adulthood, and segmental involvement is very rare. A 37-year-old man suffered from refractory constipation for 20 years.
Başar, Ömer +4 more
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Variant Hirschsprung's disease
Journal of Pediatric Surgery, 1997There are many clinical conditions that resemble Hirschsprung's disease despite the presence of ganglia cells on rectal biopsy. This group has focused its research interest into delineating variant Hirschsprung's disease based on specific histochemical, immunohistochemical, silver staining and electron microscopic studies.
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“Acquired” Hirschsprung's disease
Journal of Pediatric Surgery, 1981A case of Hirschsprung's disease is presented in which the presence of a group of ganglion cells noted on a rectal biopsy done at age 3 wk resulted in a 10-yr delay in definitive treatment.
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Hirschsprung's disease. Management
Alimentary Pharmacology & TherapeuticsSummaryBackgroundHirschsprung's disease (HD) is a rare congenital disease that is characterised by the absence of ganglion cells in the myenteric plexus starting in the distal bowel. This results in distal functional obstruction and may lead to complications like enterocolitis.
Claudio Morera, Samuel Nurko
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Surgery (Oxford), 2016
Abstract Hirschsprung's disease (HSCR) is characterized by a lack of enteric nervous system ganglion cells (aganglionosis) in a variable extent of distal bowel. It is the most common congenital bowel motility disorder and affected neonates usually present with distal intestinal obstruction in the first few days of life.
Sumita Chhabra, Simon E. Kenny
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Abstract Hirschsprung's disease (HSCR) is characterized by a lack of enteric nervous system ganglion cells (aganglionosis) in a variable extent of distal bowel. It is the most common congenital bowel motility disorder and affected neonates usually present with distal intestinal obstruction in the first few days of life.
Sumita Chhabra, Simon E. Kenny
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