Guidelines for implementation of population-based newborn screening for severe combined immunodeficiency |
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Authors: | Anne Marie Comeau Jaime E. Hale Sung-Yun Pai Francisco A. Bonilla Luigi D. Notarangelo Mark S. Pasternack H. Cody Meissner Ellen Rae Cooper Alfred DeMaria Inderneel Sahai Roger B. Eaton |
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Affiliation: | 1.New England Newborn Screening Program,UMass Medical School,Jamaica Plain,USA;2.Children’s Hospital,Boston,USA;3.Dana-Farber Cancer Institute,Boston,USA;4.Massachusetts General Hospital,Boston,USA;5.Tufts Medical Center,Boston,USA;6.Boston Medical Center,Boston,USA;7.Massachusetts Department of Public Health,Boston,USA |
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Abstract: | Severe combined immunodeficiency (SCID) is a Primary Immune Deficiency that is under consideration for population-based newborn screening (NBS) by many NBS programs, and has recently been recommended for inclusion in the US uniform panel of newborn screening conditions. A marker of SCID, the T cell receptor excision circle (TREC), is detectable in the newborn dried blood spot using a unique molecular assay as a primary screen. The New England Newborn Screening Program developed and validated a multiplex TREC assay in which both the TREC analyte and an internal control are acquired from a single punch and run in the same reaction. Massachusetts then implemented a statewide pilot SCID NBS program. The authors describe the rationale for a pilot SCID NBS program, a comprehensive strategy for successful implementation, the screening test algorithm, the screening follow-up algorithm and preliminary experience based on statewide screening in the first year. The Massachusetts experience demonstrates that SCID NBS is a program that can be implemented on a population basis with reasonable rates of false positives. |
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