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Inborn errors Congenital defects involve enzyme deficiencies in the carnitine transport or metabolic pathways, such as CPT II deficiency, which affects the function of the carnitine transporter CPT II and leads to impaired fatty acid -oxidation, and CACT deficiency, which affects the function of the carnitine transporter CACT and results in carnitine shuttle dysfunction

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410 Benzbromarone Benzbromarone, recognized as a uricosuric agent, exhibits notable in vitro inhibitory effects on urate transport facilitated by URAT1 and GLUT-9