Simultaneous newborn screening for sickle cell disease, biotinidase deficiency, and hereditary tyrosinemia type 1 with an optimized tandem mass spectrometry protocol

MeSH terms

• Anemia, Sickle Cell* / complications
• Anemia, Sickle Cell* / diagnosis
• Biotinidase Deficiency* / diagnosis
• Humans
• Infant, Newborn
• Neonatal Screening
• Tandem Mass Spectrometry / methods
• Tyrosinemias* / complications
• Tyrosinemias* / diagnosis