/autosomal dominant hyperinsulinism due to Kir6.2 deficiency

autosomal dominant hyperinsulinism due to Kir6.2 deficiency

Rare Disease

MONDO:0017185

Also Known As

autosomal dominant hyperinsulinemic hypoglycemia due to Kir6.2 deficiencydominant KATP hyperinsulinism due to Kir6.2 deficiency

Definition

Autosomal dominant hyperinsulinism due to Kir6.2 deficiency is a form of diazoxide-sensitive diffuse hyperinsulinism (DHI) characterized by hypoglycemic epiosodes that are usually mild, escaping detection during infancy, and usually a good clinical response to diazoxide, (but some are diazoxide resistant). Autosomal dominant hyperinsulinism due to Kir6.2 deficiency usually has a milder phenotype when compared to that resulting from recessive K+ (K-ATP) channel mutations (Recessive forms of diazoxide-resistant hyperinsulinism).