Congenital hyperinsulinism associated with Hirschsprung’s disease—a report of an extremely rare case
Abstract Background Congenital hyperinsulinism (CH) is a rare disease, characterized by severe hypoglycemia induced by inappropriate insulin secretion from pancreatic beta-cells in neonate and infant. Hirschsprung’s disease (HD) is also a rare disease in which infants show severe bowel movement diso...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Japan Surgical Society
2020-01-01
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| Seri Bilgileri: | Surgical Case Reports |
| Konular: | |
| Online Erişim: | https://doi.org/10.1186/s40792-020-0778-3 |
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