SUN-272 Persistent Hyperinsulinemic Hypoglycemia Due to Mutation in Hepatocyte Nuclear Factor 4A

Background: Congenital hyperinsulinism (HI) is the most common cause of hypoglycemia in children. Delay in diagnosis and or inadequate management can lead to brain damage. Persistent hyperinsulinemic hypoglycemia of infancy is a genetic disorder with both familial and sporadic form. Aim: To present...

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Detaylı Bibliyografya
Yayımlandı:J Endocr Soc
Asıl Yazarlar: Vlachopapadopoulou, Elpis, Dikaiakou, Eirini, Athanasouli, Fani, Sifianou, Popi, Sertedaki, Amalia, Michalacos, Stefanos
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Endocrine Society 2019
Konular:
Pediatric Endocrinology
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6552805/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SUN-272
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