hrp0097rfc1.4 | Adrenals and HPA Axis | ESPE2023
Francisco Annelise
, Mine Yilmaz Goler Ayse
, Daniele Carvalho Navarro Claudia
, Onder Asan
, Yildiz Melek
, Kendir Demirkol Yasemin
, Karademir Yilmaz Betul
, Seven Menevse Tuba
, Guran Tulay
, Frigério Castilho Roger
Background: Mutations in the nicotinamide nucleotide transhydrogenase (NNT) gene are a rare cause of primary adrenal insufficiency (PAI), as well as cardiomyopathies and functional impairment of the gonads.Objective: Despite the description of different NNT mutations in homozygosis and compound heterozygosis in PAI patients, it remains to be clarified to which extent the function and expression of the m...