Searchable abstracts of presentations at key conferences in endocrinology

ea0078p45 | Miscellaneous | BSPED2021

Heterozygous mutations in ATP-sensitive potassium channel (KATP) genes associated with transient and mild hyperinsulinaemic hypoglycaemia

Siese Thomas , Alins-Sahun Yolanda , Crowne Elizabeth , Giri Dinesh

Introduction: Congenital hyperinsulinism (CHI) is a rare disease, characterized by an unregulated insulin release, leading to hypoglycaemia. It is the most frequent cause of persistent and severe hypoglycaemia during the neonatal period and early childhood. Mutations in KATP < genes (ABCC8 and KCNJ11), together account for up to 70% of CHI. CHI can either be transient or persistent. Transient CHI tends to resolve spontaneously and is n...