hrp0095p1-206 | Adrenals and HPA Axis | ESPE2022
Dursun Fatma
, Maras Genc Hulya
, Mine Yılmaz Ayşe
, Tas Ibrahim
, Eser Metin
, Pehlivanoglu Cemile
, Karademir Yilmaz Betul
, Guran Tulay
Background: Biallelic QRSL1 mutations cause mitochondrial “combined oxidative phosphorylation deficiency-40” (COXPD40). COXPD40 has been reported invariably lethal in infancy. Adrenal insufficiency was weakly reported and investigated among seven previously reported patients with COXPD40.Objective: We report clinical, biochemical, molecular, and functional characteristics of a patient with adrenal in...