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Case report: Congenital hyperinsulinemia with ABCC8 gene mutations
BACKGROUND: Congenital hyperinsulinemia (CHI) is an inherited disease of abnormal insulin secretion and is the main cause of persistent and intractable hypoglycemia in infants. The aim of this case report was to investigate the genetic mechanisms and treatment of CHI in an affected patient. CASE SUM...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403267/ https://www.ncbi.nlm.nih.gov/pubmed/36034573 http://dx.doi.org/10.3389/fped.2022.914267 |