Searchable abstracts of presentations at key conferences in endocrinology

ea0056p87 | Clinical case reports - Pituitary/Adrenal | ECE2018

Long-term follow-up of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

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...