Hirschsprung's disease in a genetically diagnosed Cri-du-chat syndrome baby
Introduction: Hirschsprung's disease (HSD) is a congenital disease characterized by the absence of ganglion cells in the myenteric and submucosal plexuses of the gastrointestinal tract. Many genetic causes of HSD have been investigated, although the most common and widely accepted is the RET ge...
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| Autores principales: | , , , , |
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| Formato: | Libro |
| Publicado: |
Elsevier,
2023-04-01T00:00:00Z.
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| Acceso en línea: | Connect to this object online. |
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| Número de Clasificación: |
A1234.567 |
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| Copia 1 | Disponible |