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J Pediatr ; 195: 283-287, 2018 04.
Article in English | MEDLINE | ID: mdl-29273175

ABSTRACT

We conducted an inventory of state-based recommendations for follow-up of alpha thalassemia silent carrier and trait identified on newborn screen. We found wide variability in the nature and timing of these recommendations. We recommend a standardized recommendation to guide pediatricians in evidenced-based care for this population.


Subject(s)
Aftercare/standards , Heterozygote , Neonatal Screening , alpha-Thalassemia/therapy , Cross-Sectional Studies , Humans , Infant , Infant, Newborn , Practice Guidelines as Topic , United States , alpha-Thalassemia/diagnosis , alpha-Thalassemia/genetics
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