Familial Hyperinsulinism due to HNF4A Deficiency and Benign Premature Adrenarche: A Case Report

Familial Hyperinsulinism due to HNF4A Deficiency and Benign Premature Adrenarche: A Case Report

Background: Familial Hyperinsulinism due to HNF4A deficiency (FHI-HNF4A) is a form of diazoxide-sensitive, diffuse hyperinsulinism, characterized by transient or persistent hyperinsulinemic hypoglycemia, and a propensity to develop Maturity-Onset Diabetes of the Young type 1 (MODY1). The associatio...

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Bibliographic Details
Main Authors: Edward Compton, David H. Geller, Alaina Vidmar
Format: Article
Language:English
Published: University Library System, University of Pittsburgh 2021-05-01
Series:International Journal of Medical Students
Subjects:
Hyperinsulinism
Congenital hyperinsulinism
Adrenarche
HNF4A
Hyperandrogenism
Online Access:https://ijms.info/IJMS/article/view/721

Internet

https://ijms.info/IJMS/article/view/721

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