Congenital Hyperinsulinism


Congenital Hyperinsulinisms

Familial Hyperinsulinemic Hypoglycemia 1

Familial Hyperinsulinism

Familial Hyperinsulinisms

Hyperinsulinemia Hypoglycemia of Infancy

Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia

Hyperinsulinemic Hypoglycemia, Familial, 1

Hyperinsulinemic Hypoglycemia, Familial, 2

Hyperinsulinemic Hypoglycemia, Persistent

Hyperinsulinemic Hypoglycemias, Persistent

Hyperinsulinism, Congenital

Hyperinsulinism, Familial

Hyperinsulinism, Neonatal

Hyperinsulinisms, Congenital

Hyperinsulinisms, Familial

Hyperinsulinisms, Neonatal

Hypoglycemia, Hyperinsulinemic, of Infancy

Hypoglycemia, PHHI

Hypoglycemia, Persistent Hyperinsulinemic

Hypoglycemias, PHHI

Hypoglycemias, Persistent Hyperinsulinemic

Infancy Hyperinsulinemia Hypoglycemia

Infancy Hyperinsulinemia Hypoglycemias

Neonatal Hyperinsulinism

Neonatal Hyperinsulinisms

PHHI Hypoglycemia

PHHI Hypoglycemias

Persistent Hyperinsulinemia Hypoglycemia of Infancy

Persistent Hyperinsulinemic Hypoglycemia

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).