Congenital aganglionic megacolon; (Hirschsprung's disease).
Tex State J Med. 1957.
PMID: 13467819
No abstract available.
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5
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found by citation matching
Image and diagnosis. Hirschsprung disease (congenital aganglionic megacolon).
West Indian Med J. 2003.
PMID: 15040071
No abstract available.
Congenital aganglionic megacolon; Hirschsprung's disease.
AMA Am J Dis Child. 1955.
PMID: 13268054
No abstract available.
Search results
Page 1
Hirschsprung's disease: diagnosis and management.
Am Fam Physician. 2006 Oct 15;74(8):1319-22.
Am Fam Physician. 2006.
PMID: 17087425
Free article.
Review.
Hirschsprung's disease (congenital megacolon) is caused by the failed migration of colonic ganglion cells during gestation. ...Patients should be monitored closely for enterocolitis for years after surgical treatment of Hirschsprung's disease …
Hirschsprung's disease (congenital megacolon) is caused by the failed migration of colonic ganglion cells during …
Hirschsprung's Disease-Recent Understanding of Embryonic Aspects, Etiopathogenesis and Future Treatment Avenues.
Medicina (Kaunas). 2020 Nov 13;56(11):611. doi: 10.3390/medicina56110611.
Medicina (Kaunas). 2020.
PMID: 33202966
Free PMC article.
Review.
From the diagnostic perspective, researchers also focused on "Variants of Hirschsprung's disease", which can mimic the clinical signs of the disease, but are in fact different entities, with distinct prognosis and treatment approaches. The treatment of Hir …
From the diagnostic perspective, researchers also focused on "Variants of Hirschsprung's disease", which can mimic the clinica …
The science of Hirschsprung disease: What we know and where we are headed.
Semin Pediatr Surg. 2022 Apr;31(2):151157. doi: 10.1016/j.sempedsurg.2022.151157. Epub 2022 Apr 18.
Semin Pediatr Surg. 2022.
PMID: 35690468
Review.
Hirschsprung disease is a congenital neurocristopathy, a disease of the neural crest. It is characterized by a variable length of distal colonic aganglionosis due to a failure in enteric neural crest-derived cell proliferation, migration, differentiati …
Hirschsprung disease is a congenital neurocristopathy, a disease of the neural crest. It is characterized by a v …
The developmental etiology and pathogenesis of Hirschsprung disease.
Transl Res. 2013 Jul;162(1):1-15. doi: 10.1016/j.trsl.2013.03.001. Epub 2013 Mar 22.
Transl Res. 2013.
PMID: 23528997
Free PMC article.
Review.
Disorders that arise as a consequence of defective neural crest cell development are termed neurocristopathies. One such disorder is Hirschsprung disease (HSCR), also known as congenital megacolon or intestinal aganglionosis. ...The inheritance of HSCR …
Disorders that arise as a consequence of defective neural crest cell development are termed neurocristopathies. One such disorder is Hirs …
ERNICA guidelines for the management of rectosigmoid Hirschsprung's disease.
Orphanet J Rare Dis. 2020 Jun 25;15(1):164. doi: 10.1186/s13023-020-01362-3.
Orphanet J Rare Dis. 2020.
PMID: 32586397
Free PMC article.
Review.
BACKGROUND: Hirschsprung's disease (HSCR) is a serious congenital bowel disorder with a prevalence of 1/5000. ...It aims to describe the preferred approach of ERNICA, the European Reference Network for rare inherited and congenital digestive disorders. …
BACKGROUND: Hirschsprung's disease (HSCR) is a serious congenital bowel disorder with a prevalence of 1/5000. ...It aim …
Intestinal fibrosis in aganglionic segment of Hirschsprung's disease revealed by single-cell RNA sequencing.
Clin Transl Med. 2023 Feb;13(2):e1193. doi: 10.1002/ctm2.1193.
Clin Transl Med. 2023.
PMID: 36738110
Free PMC article.
BACKGROUND: Hirschsprung's disease (HSCR) is a relatively common congenital disability. ...The fibrotic regulators POSTN, ANXA1 and HSP70 were highly expressed in the ECM-related cellular subsets in the transitional segments and aganglionic segments. T …
BACKGROUND: Hirschsprung's disease (HSCR) is a relatively common congenital disability. ...The fibrotic regulators POST …
Hirschsprung disease.
Curr Opin Pediatr. 2013 Jun;25(3):368-74. doi: 10.1097/MOP.0b013e328360c2a0.
Curr Opin Pediatr. 2013.
PMID: 23615177
Review.
PURPOSE OF REVIEW: Hirschsprung disease is relatively common in children. Surgical techniques are available to remove the aganglionic bowel and reconstruct the intestinal tract. ...SUMMARY: Pediatricians and primary care physicians have an important role to p …
PURPOSE OF REVIEW: Hirschsprung disease is relatively common in children. Surgical techniques are available to remove the a …
Hirschsprung Disease.
Pediatr Rev. 2021 Dec 1;42(12):714-716. doi: 10.1542/pir.2020-004912.
Pediatr Rev. 2021.
PMID: 36017952
No abstract available.
Per rectal endoscopic myotomy for Hirschsprung's disease and megacolon.
Minerva Gastroenterol (Torino). 2023 Jun;69(2):175-183. doi: 10.23736/S2724-5985.22.03166-7. Epub 2022 Mar 28.
Minerva Gastroenterol (Torino). 2023.
PMID: 35343667
Review.
Hirschsprung's disease (HD) is a congenital disorder characterized by absence of intrinsic ganglion cells of the hindgut. ...Per-rectal endoscopic myotomy (PREM) is a recently described novel minimally invasive procedure based on the principles of third space …
Hirschsprung's disease (HD) is a congenital disorder characterized by absence of intrinsic ganglion cells of the hindgu …
Fecal microbiota transplantation enhances cell therapy in a rat model of hypoganglionosis by SCFA-induced MEK1/2 signaling pathway.
EMBO J. 2023 Jan 4;42(1):e111139. doi: 10.15252/embj.2022111139. Epub 2022 Nov 16.
EMBO J. 2023.
PMID: 36382711
Free PMC article.
Hirschsprung disease (HSCR), one of several neurocristopathies in children, is characterized by nerve loss in the large intestine and is mainly treated by surgery, which causes severe complications. ...
Hirschsprung disease (HSCR), one of several neurocristopathies in children, is characterized by nerve loss in the large intest …
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