Congenital hyperinsulinism associated with Hirschsprung’s disease—a report of an extremely rare case

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 disorder. We...

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Detalles Bibliográficos
Autores principales: Shono, Takeshi, Shono, Kumiko, Hashimoto, Yoshiko, Taguchi, Shohei, Masuda, Masanori, Muramori, Kastumi, Taguchi, Tomoaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949352/
https://www.ncbi.nlm.nih.gov/pubmed/31916119
http://dx.doi.org/10.1186/s40792-020-0778-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949352/
https://www.ncbi.nlm.nih.gov/pubmed/31916119
http://dx.doi.org/10.1186/s40792-020-0778-3

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