Congenital Hyperinsulinism

Familial Hyperinsulinemic Hypoglycemia 1
Familial Hyperinsulinism
Hyperinsulinemia Hypoglycemia of Infancy
Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia
Hyperinsulinemic Hypoglycemia, Familial, 1
Hyperinsulinemic Hypoglycemia, Familial, 2
Hyperinsulinemic Hypoglycemia, Persistent
Hyperinsulinism, Congenital
Hyperinsulinism, Familial
Hyperinsulinism, Neonatal
Hypoglycemia, Hyperinsulinemic, of Infancy
Infancy Hyperinsulinemia Hypoglycemia
Neonatal Hyperinsulinism
PHHI Hypoglycemia
Persistent Hyperinsulinemic Hypoglycemia
Persistent Hyperinsulinemia Hypoglycemia of Infancy
Congenital Hyperinsulinisms
Familial Hyperinsulinisms
Hyperinsulinemic Hypoglycemias, Persistent
Hyperinsulinisms, Congenital
Hyperinsulinisms, Familial
Hyperinsulinisms, Neonatal
Hypoglycemia, PHHI
Hypoglycemia, Persistent Hyperinsulinemic
Hypoglycemias, PHHI
Hypoglycemias, Persistent Hyperinsulinemic
Infancy Hyperinsulinemia Hypoglycemias
Neonatal Hyperinsulinisms
PHHI Hypoglycemias
Persistent Hyperinsulinemic Hypoglycemias

A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMIA; HYPERINSULINEMIA; SEIZURES; COMA; and often large BIRTH WEIGHT. Several sub-types exist with the most common, type 1, associated with mutations on an ATP-BINDING CASSETTE TRANSPORTERS (subfamily C, member 8).
2014(2004)