Congenital isolated hyperinsulinism

Overview

What else is congenital isolated hyperinsulinism called?

Congenital isolated hyperinsulinism is also known by the following names

  • Persistent hyperinsulinemic hypoglycemic of infancy
  • Congenital hyperinsulinism
  • Familial hyperinsulinemic hypoglycemia
  • Primary isent cell hypertrophy (nesidioblastosis)

Glaser B. Familial Hyperinsulinism. Gene Reviews. 2016; https://www.ncbi.nlm.nih.gov/books/NBK1375/. Congenital Hyperinsulinism. National Organization for Rare Diseases (NORD). 2016; https://rarediseases.org/rare-diseases/congenital-hyperinsulinism/ Sunehag A & Haymond MW. Pathogenesis, clinical features, and diagnosis of persistent hyperinsulinemic hypoglycemia of infancy. UpToDate. 2018; http://www.uptodate.com/contents/pathogenesis-clinical-features-and-diagnosis-of-persistent-hyperinsulinemic-hypoglycemia-of-infancy.

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