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Author

Salma Abouchiba

2 papers indexed here

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Case report Open access Aug 2026

Incidental discovery of neglected 11β-hydroxylase deficiency causing 46,XX disorder of sex development in a 35-year-old adult: A radiologically driven diagnosis

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. · 0 citations
Open access Aug 2026

MRI Evaluation of a 46, XX Disorder of Sex Development Due to Classical 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia in a 6-Month-Old Infant: A Case Report

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. · 0 citations

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