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
MRI is a valuable, non-irradiating modality for the comprehensive evaluation of internal genitourinary anatomy in 46,XX DSD secondary to CAH, providing essential information for sex assignment, surgical planning, and multidisciplinary management decisions.
Zaid Ennasery, Salma Abouchiba, Hajar El Ouazzani et al.· World Journal of Advanced Re...· 0 citations
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