Congenital hyperinsulinism due to mutations in HNF4A and HADH. Review uri icon

Overview

abstract

  • Mutations in the HADH and HNF4A genes are rare causes of diazoxide responsive congenital hyperinsulinism (CHI). This chapter details the phenotype known to be associated with mutations in these genes. Additionally, the authors give a brief overview of the role of these genes in glucose physiology and the possible mechanisms of CHI in patients with mutations in these genes.

publication date

  • September 1, 2010

Research

keywords

  • 3-Hydroxyacyl CoA Dehydrogenases
  • Congenital Hyperinsulinism
  • Hepatocyte Nuclear Factor 4
  • Mutation

Identity

Scopus Document Identifier

  • 78650585349

Digital Object Identifier (DOI)

  • 10.1007/s11154-010-9148-y

PubMed ID

  • 20931292

Additional Document Info

volume

  • 11

issue

  • 3