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...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:Frontiers in Pediatrics
المؤلفون الرئيسيون: Mariangela Martino, Jacopo Sartorelli, Vincenza Gragnaniello, Alberto Burlina
التنسيق: مقال
اللغة:الإنجليزية
منشور في: Frontiers Media S.A. 2022-09-01
الموضوعات:
hypoglycemia
hyperinsulinism
glucose
CGM
inborn error of metabolism
الوصول للمادة أونلاين:https://www.frontiersin.org/articles/10.3389/fped.2022.901338/full

الانترنت

https://www.frontiersin.org/articles/10.3389/fped.2022.901338/full

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