| Literature DB >> 32579701 |
Johannes Trück1, Seraina Prader1, Giancarlo Natalucci2, Cornelia Hagmann1, Barbara Brotschi1, Janet Kelly1, Dirk Bassler2, Katharina Steindl3, Anita Rauch3, Matthias Baumgartner1, Ralph Fingerhut1, Mathias Hauri-Hohl1, Tayfun Güngör1, Jana Pachlopnik Schmid1, Christoph Berger1, Janine Reichenbach1.
Abstract
The recent introduction of newborn screening for severe primary T and B cell deficiencies in Switzerland allows rapid identification of patients with severe combined immunodeficiency (SCID). Outcomes for SCID are greatly improved by early diagnosis and treatment with allogeneic haematopoietic stem cell transplantation or, in selected cases, gene therapy. National centralised newborn screening is performed in Switzerland since January 2019 using a combined T cell receptor excision circles (TREC) / κ-deleting recombination excision circles (KREC) assay, also revealing infants with non-SCID severe T and B cell disorders, who are often diagnosed with a substantial delay. Here, we outline the screening procedure currently performed in Switzerland and give recommendations for diagnostic evaluations and precautionary measures against infection in children with abnormal screening test results.Entities:
Year: 2020 PMID: 32579701 DOI: 10.4414/smw.2020.20254
Source DB: PubMed Journal: Swiss Med Wkly ISSN: 0036-7672 Impact factor: 2.193