Tuberous sclerosis complex (TSC) is a rare multisystem genetic disorder characterized by hamartomatous lesions affecting multiple organs, most commonly the brain, kidneys, skin, heart, and lungs. Although typically diagnosed in childhood, late-onset presentations may occur, particularly when renal manifestations predom...
Kawtar Khaissidi, I. Chaouche, H. Ouazzani et al.· World Journal of Advanced Re...· 0 citations
Hydatid disease, or cystic echinococcosis, is a parasitic zoonosis caused by the larval stage of Echinococcus granulosus and remains endemic in Morocco. Although the liver and lungs account for most cases, the parasite may lodge in any organ or soft tissue, where it mimics a wide range of benign and malignant lesions....
M. El Mekhtoume, Ennejjari Nahla, Moulayemin Beddy et al.· World Journal of Advanced Re...· 0 citations
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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