ea0039ep84 | Miscellaneous/other | BSPED2015
Ersoy Betul
, Tansug Nermin
, Genc Abdulkadir
, Kizilay Deniz
, Kiremitci Semiha
, Ayhan Semin
, Lonlay Pascale D E
Introduction: Congenital hyperinsulinism (CHI), is the most frequent cause of persistent hypoglycemia in infancy. Mutations in the ABCC8 gene are responsible for 4050% of CHI cases. Its management can be extremely complicated. The main goal of the treatment is to maintain normoglycemia, since hypoglycemia during infancy can have severe neurological consequences. Herein, we report 8 year follow up of twin patients who were diagnosed with CHI at neonatal period due to SUR1...