The loss of calretinin expression indicates aganglionosis in Hirschsprung’s disease

Background: Hirschsprung’s disease (HD) is a congenital disorder characterised by the absence of ganglion cells in the large bowel, leading to functional obstruction and colonic dilatation proximal to the affected segment. A subclass of nerve cell bodies in both submucosa and myenteric ganglia of th...

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Bibliographic Details
Main Authors: Barshack, I, Fridman, E, Goldberg, I, Chowers, Y, Kopolovic, J
Format: Artigo
Language:Inglês
Published: Copyright 2004 Journal of Clinical Pathology 2004
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Original Articles
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1770342/
https://ncbi.nlm.nih.gov/pubmed/15220363
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jcp.2004.016030
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