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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Detalhes bibliográficos
Publicado no:Surg Case Rep
Principais autores: Shono, Takeshi, Shono, Kumiko, Hashimoto, Yoshiko, Taguchi, Shohei, Masuda, Masanori, Muramori, Kastumi, Taguchi, Tomoaki
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2020
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6949352/
https://ncbi.nlm.nih.gov/pubmed/31916119
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40792-020-0778-3
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