Overview of Tyrosinemia Type 1: Navigating a Rare Genetic Disorder
Dietary restrictions for phenylalanine and tyrosine are commonly recommended in addition to Nitisinone. Patients withContinue Reading
Dietary restrictions for phenylalanine and tyrosine are commonly recommended in addition to Nitisinone. Patients withContinue Reading
Type 1B Oculocutaneous Albinism (OCA) is a rare genetic disorder that affects individuals’ pigmentation, causingContinue Reading
The FDA-approved drug nitisinone treats hereditary tyrosinemia type 1 (HT-1), a rare genetic condition that alters howContinue Reading