ea0081ep41 | Adrenal and Cardiovascular Endocrinology | ECE2022
Mona Rekik
, Sonda Kammoun
, Omar Ayedi
, Akid Faten Haj Kacem
, Saloua Ben Amor
, Amira Trigui
Introduction: 11-Hydroxylase deficiency is a rare form of congenital adrenal hyperplasia characterized by glucocorticoid deficiency, hypertension, hypokalemia and virilization in females. We report a case of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency revealed by bilateral papilledema in the context of arterial hypertension.Case report: A 13-year-old patient, with no medical history, presented with complains of headache, vomiting ...