NHS Expands Newborn Screening for Rare Metabolic Disorder
The NHS now screens all newborns for Hereditary Tyrosinaemia Type 1 (HT1), a rare, life-threatening metabolic disorder. Early detection prevents severe complications and improves outcomes.
The NHS now screens all newborns for Hereditary Tyrosinaemia Type 1 (HT1), a rare, life-threatening metabolic disorder. Early detection prevents severe complications and improves outcomes.