Congenital Hyperinsulinism
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).
Year introduced: 2014(2004)
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Tree Number(s): C06.689.150, C16.614.200, C18.452.394.968.250, C18.452.394.984.200
MeSH Unique ID: D044903
Entry Terms:
- Congenital Hyperinsulinisms
- Hyperinsulinisms, Congenital
- Familial Hyperinsulinism
- Hyperinsulinemia Hypoglycemia of Infancy
- Infancy Hyperinsulinemia Hypoglycemias
- Hyperinsulinemic Hypoglycemia, Persistent
- Hyperinsulinemic Hypoglycemias, Persistent
- Hypoglycemia, Persistent Hyperinsulinemic
- Hypoglycemias, Persistent Hyperinsulinemic
- Persistent Hyperinsulinemic Hypoglycemias
- Hyperinsulinism, Congenital
- Hyperinsulinism, Familial
- Familial Hyperinsulinisms
- Hyperinsulinisms, Familial
- Hyperinsulinism, Neonatal
- Hyperinsulinisms, Neonatal
- Neonatal Hyperinsulinisms
- Hypoglycemia, Hyperinsulinemic, of Infancy
- Infancy Hyperinsulinemia Hypoglycemia
- Neonatal Hyperinsulinism
- Persistent Hyperinsulinemia Hypoglycemia of Infancy
- Persistent Hyperinsulinemic Hypoglycemia
- PHHI Hypoglycemia
- Hypoglycemia, PHHI
- Hypoglycemias, PHHI
- PHHI Hypoglycemias
- Hyperinsulinemic Hypoglycemia, Familial, 2
- Familial Hyperinsulinemic Hypoglycemia 1
- Hyperinsulinemic Hypoglycemia Due to Focal Adenomatous Hyperplasia
- Hyperinsulinemic Hypoglycemia, Familial, 1
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