Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare form of congenital diazoxide-sensitive diffuse hyperinsulinism due to UCP2 deficiency and characterized by hypoglycemic episodes from the neonatal period, a good clinical response to diazoxide and a probable transient nature of the disease with spontaneous resolution. Disease data Classification Disease Synonyms Hyperinsulinemic hypoglycemia due to UCP2 deficiency Hipoglikemia hiperinsulinemiczna z powodu niedoboru UCP2 ORPHA code 276556 OMIM code - ICD10 code E16.1 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl