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...
| Hlavní autoři: | , , , |
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| Médium: | Článek |
| Jazyk: | English |
| Vydáno: |
Frontiers Media S.A.
2022-09-01
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| Edice: | Frontiers in Pediatrics |
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| On-line přístup: | https://www.frontiersin.org/articles/10.3389/fped.2022.901338/full |