Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor

N Engl J Med. 1997 Mar 6;336(10):703-6. doi: 10.1056/NEJM199703063361005.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • ATP-Binding Cassette Transporters*
  • Female
  • Humans
  • Hyperinsulinism / genetics*
  • Hypoglycemia / genetics*
  • Infant, Newborn
  • Insulin / metabolism
  • Insulin Secretion
  • Islets of Langerhans / metabolism
  • Mutation
  • Potassium Channels / genetics*
  • Potassium Channels / physiology
  • Potassium Channels, Inwardly Rectifying*
  • Receptors, Drug / genetics*
  • Receptors, Drug / physiology
  • Sulfonylurea Compounds
  • Sulfonylurea Receptors

Substances

  • ATP-Binding Cassette Transporters
  • Insulin
  • Potassium Channels
  • Potassium Channels, Inwardly Rectifying
  • Receptors, Drug
  • Sulfonylurea Compounds
  • Sulfonylurea Receptors