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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Vydáno v:Iran J Pathol
Hlavní autoři: Rakhshani, Nasser, Araste, Mohammadreza, Imanzade, Farid, Panahi, Mahshid, Safarnezhad Tameshkel, Fahimeh, Sohrabi, Masoud Reza, Karbalaie Niya, Mohammad Hadi, Zamani, Farhad
Médium: Artigo
Jazyk:Inglês
Vydáno: Iranian Society of Pathology 2016
Témata:
Short Communication
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5563939/
https://ncbi.nlm.nih.gov/pubmed/28855933
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