ea0056p87 | Clinical case reports - Pituitary/Adrenal | ECE2018
Elfekih Hamza
, Hasni Yosra
, Badr Wafa
, Abdelkrim Asma Ben
, Amor Bilel Ben
, Maaroufi Amal
, Kacem Maha
, Chaieb Molka
, Gribaa Moez
, Ach Koussay
, Saad Ali
Introduction: Congenital adrenal hyperplasia (CAH) due to an enzymatic defect in 11-beta-hydroxylase (11β-OHD) is the second most common cause of CAH representing 5-8% of cases. It is characterized by androgen excess, hypertension and hypokalemia. Here we describe the case of a patient having a CYP11B1 mutation and being followed-up during 33 years.Observation: A 36-year-old Tunisian male was diagnosed with 11β-OHD at the age of three years rev...