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

Authors :: Lobitz S
Frömmel C
Brose A
Blankenstein O
Turner C
Dalton RN
Daniel Y
Klein J
Source :: Annals of hematology [Ann Hematol] 2022 Aug; Vol. 101 (8), pp. 1859-1860. Date of Electronic Publication: 2022 Mar 16.
Publication Year :: 2022

Subjects :: Humans
Infant, Newborn
Neonatal Screening
Tandem Mass Spectrometry methods
Anemia, Sickle Cell complications
Anemia, Sickle Cell diagnosis
Biotinidase Deficiency diagnosis
Tyrosinemias complications
Tyrosinemias diagnosis

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