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Hyperinsulinemic hypoglycemia, familial, 3

rare

A form of diffuse hyperinsulinism due to glucokinase hyperactivity associated with a variation in the GCK gene, and characterized by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia) and recurrent episodes of hypoglycemia induced by fasting and glucose rich meals.

Identifiers
MONDO:0011236 OMIM:602485Orphanet:79299
Causal genes
GCK
Part of
Congenital isolated hyperinsulinismDisorder of glycolysis
Also known as
congenital glucokinase-related hyperinsulinism · GCK-related hyperinsulinism · glucokinase-related hyperinsulinemic hypoglycemia · HHF3 · hyperinsulinemic hypoglycemia familial 3

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