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Newborn Screening for Phenylketonuria
Author(s) -
Gustavo Borrajo
Publication year - 2016
Publication title -
journal of inborn errors of metabolism and screening
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.125
H-Index - 5
eISSN - 2326-4594
pISSN - 2326-4098
DOI - 10.1177/2326409816682764
Subject(s) - context (archaeology) , newborn screening , latin americans , pediatrics , national laboratory , dried blood , blood collection , medicine , geography , political science , emergency medicine , chemistry , engineering , engineering physics , chromatography , law , archaeology
Newborn screening (NBS) for phenylketonuria in Latin America gave its first step in an organized way 3 decades ago when the first national NBS program was implemented in Cuba. From then onward, it experienced a slow but continuous growing, being currently possible to find from countries where no NBS activity is known to several countries with consolidated NBS programs. This complex scenario gave rise to a great diversity in the criteria used for sample collection, selection of analytical methods, and definition of cutoff values. Considering this context, a consensus meeting was held in order to unify such criteria, focusing the discussion in the following aspects—recommended blood specimens and sample collection time; influence of early discharge, fasting, parenteral nutrition, blood transfusions, extracorporeal life support, and antibiotics; main causes of transient hyperphenylalaninemias; required characteristics for methods used in phenylalanine measurement; and finally, criteria to define the more appropriate cutoff values

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