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...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Iranian Society of Pathology
2016-10-01
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Series: | Iranian Journal of Pathology |
Subjects: | |
Online Access: | https://ijp.iranpath.org/article_22235_43b01f54f65ec0bc3e4d3a4347f0e5ab.pdf |