Tag: Biotinidase deficiency

Biotinidase deficiency, a rare inherited metabolic disorder, is detected in approximately 1 in 61,067 newborns worldwide through mandatory screening programs. This condition, if left untreated, can cause severe neurological and dermatological issues, making it critical to understand **what medication is used for biotinidase** to prevent serious complications.

Did you know that high doses of biotin can cause dangerously inaccurate results in vital lab tests, including those for thyroid and heart disease? Understanding who cannot take biotin and the associated risks is crucial for patient safety and proper medical management, requiring caution even for those seeking hair, skin, and nail benefits.