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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Detalles Bibliográficos
Autores principales: Rakhshani, Nasser, Araste, Mohammadreza, Imanzade, Farid, Panahi, Mahshid, Safarnezhad Tameshkel, Fahimeh, Sohrabi, Masoud Reza, Karbalaie Niya, Mohammad Hadi, Zamani, Farhad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Society of Pathology 2016
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5563939/
https://www.ncbi.nlm.nih.gov/pubmed/28855933

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5563939/
https://www.ncbi.nlm.nih.gov/pubmed/28855933

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