A Rare Presentation of Classical Homocystinuria: Cerebral Thrombophlebitis in an Adolescent
Noura Agarrab, Asmae Baaziz, Imane Zineb & Asmaa Mdaghri Alaoui · Asian Journal of Advanced Research and Reports · 2025
Homocystinuria is a rare constitutional aminoacidopathy characterized by elevated plasma and urinary homocysteine levels, most often due to cystathionine beta-synthase (CBS) deficiency, and represents the second most frequent metabolic encephalopathy after phenylketonuria. We rep...
Open access
Research Article
10.9734/ajarr/2025/v19i101185