Hirschsprung Disease Diagnosis: Calretinin Marker Role in Determining the Presence or Absence of Ganglion Cells

Background: Hirschsprung disease is a complex genetic disorder of the enteric nervous system (ENS), often called congenital aganglionic megacolon and characterized by the absence of enteric neurons along a variable length of the intestine. The definitive diagnosis of Hirschsprung disease relies on h...

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Bibliographic Details
Main Authors: Nasser Rakhshani, Mohammadreza Araste, Farid Imanzade, Mahshid Panahi, Fahimeh Safarnezhad Tameshkel, Masoud Reza Sohrabi, Mohammad Hadi Karbalaie Niya, Farhad Zamani
Format: Article
Language:English
Published: Iranian Society of Pathology 2016-10-01
Series:Iranian Journal of Pathology
Subjects:
Online Access:https://ijp.iranpath.org/article_22235_43b01f54f65ec0bc3e4d3a4347f0e5ab.pdf