11β-hydroxylase deficiency (11β-OHD) is the second most common form of congenital adrenal hyperplasia (CAH), characterized by androgen excess, mineralocorticoid-driven hypertension, and hypokalemia. We report a 35-year-old individual with a 46,XX karyotype, registered and raised male since birth, in whom a disorder of...
Salma Abouchiba, N. Ennejjari, H. Ouazzani et al.· Radiology Case Reports· 0 citations
Background: Classical congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is the most common cause of 46,XX disorders of sex development (DSD), resulting in androgenic virilization of the female external genitalia. Magnetic resonance imaging (MRI) plays a central and increasingly indispensable role in...
Zaid Ennasery, Salma Abouchiba, Hajar El Ouazzani et al.· World Journal of Advanced Re...· 0 citations
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