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.
Original language | English (US) |
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Pages (from-to) | 283-287 |
Number of pages | 5 |
Journal | Journal of Pediatrics |
Volume | 195 |
DOIs | |
State | Published - Apr 2018 |
All Science Journal Classification (ASJC) codes
- Pediatrics, Perinatology, and Child Health