hyperinsulinaemic hypoglycaemia type 5
hyperinsulinaemic hypoglycaemia type 5
An autosomal dominant condition (OMIM:609968) characterised by persistent hypoglycaemia in infancy due to defective negative feedback regulation of insulin secretion by low serum glucose levels.Molecular pathology
Defects of INSR cause hyperinsulinaemic hypoglycaemia type 5.