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Congenital hyperinsulinism in clinical practice: From biochemical pathophysiology to new monitoring techniques
Congenital hyperinsulinism comprises a group of diseases characterized by a persistent hyperinsulinemic hypoglycemia, due to mutation in the genes involved in the regulation of insulin secretion. The severity and the duration of hypoglycemic episodes, primarily in the neonatal period, can lead to ne...
| 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/PMC9538154/ https://www.ncbi.nlm.nih.gov/pubmed/36210928 http://dx.doi.org/10.3389/fped.2022.901338 |