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• W2767366282 abstract "The primary objective of population-based newborn screening is the early identification of asymptomatic infants with a range of severe diseases, for which effective treatment is available and where early diagnosis and intervention prevent serious sequelae. Primary immunodeficiency diseases (PID) are a heterogeneous group of inborn errors of immunity. Severe combined immunodeficiency (SCID) is one form of PID which is uniformly fatal without early, definitive therapy, and outcomes are significantly improved if infants are diagnosed and treated within the first few months of life. Screening for SCID using T cell receptor excision circle (TREC) analysis has been introduced in many countries worldwide. The utility of additional screening with kappa recombining excision circles (KREC) has also been described, enabling identification of infants with severe forms of PID manifested by T and B cell lymphopenia. Here, we review the early origins of newborn screening and the evolution of screening methodologies. We discuss current strategies employed in newborn screening programs for PID, including TREC and TREC/KREC-based screening, and consider the potential future role of protein-based assays, targeted sequencing, and next generation sequencing (NGS) technologies, including whole genome sequencing (WGS)." @default.
• W2767366282 created "2017-11-17" @default.
• W2767366282 creator A5008915149 @default.
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• W2767366282 date "2017-11-08" @default.
• W2767366282 modified "2023-10-12" @default.
• W2767366282 title "Newborn Screening for Primary Immunodeficiency Diseases: History, Current and Future Practice" @default.
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• W2767366282 doi "https://doi.org/10.1007/s10875-017-0455-x" @default.
• W2767366282 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5742602" @default.
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