Hirschsprung’s Disease in Neonates with Special Reference to Calretinin Immunohistochemistry
Background: Hirschsprung’s disease is a classic example of a complex genetic disease, characterized by the lack of enteric ganglia in the submucosal and myenteric plexuses, along variable portions of the distal gut. The diagnosis of Hirschsprung’s disease is based on a combination of clinical f...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
JCDR Research and Publications Private Limited
2015-07-01
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| Schriftenreihe: | Journal of Clinical and Diagnostic Research |
| Schlagworte: | |
| Online-Zugang: | https://jcdr.net/articles/PDF/6180/12470_CE[Ra1]_F(AK)_PF1(PAK)_PFA(AK)_PFA2(AK)_PF2(PAG).pdf |
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