Literature DB >> 26366807

Newborn screening for cystic fibrosis.

Tanja Gonska1,2, Felix Ratjen2,3.   

Abstract

Newborn screening for cystic fibrosis (CF NBS) has been introduced in almost all of the Western countries, and most of the children with CF are now being identified via CF NBS before disease-related symptoms develop. This review summarizes the evidence that has been generated to date to support the benefit of CF NBS and the various screening algorithms that are used in different jurisdictions. A special focus is directed towards the challenges arising from false-negative and -positive screening results. Finally, we review the emerging data reporting on positively-screened newborns, in whom confirmatory sweat testing resulted in an inconclusive diagnosis for CF.

Entities:  

Keywords:  cystic fibrosis; nbs; positive screened newborns with inconclusive diagnosis

Mesh:

Year:  2015        PMID: 26366807     DOI: 10.1586/17476348.2015.1085804

Source DB:  PubMed          Journal:  Expert Rev Respir Med        ISSN: 1747-6348            Impact factor:   3.772


  3 in total

Review 1.  The future of cystic fibrosis care: a global perspective.

Authors:  Scott C Bell; Marcus A Mall; Hector Gutierrez; Milan Macek; Susan Madge; Jane C Davies; Pierre-Régis Burgel; Elizabeth Tullis; Claudio Castaños; Carlo Castellani; Catherine A Byrnes; Fiona Cathcart; Sanjay H Chotirmall; Rebecca Cosgriff; Irmgard Eichler; Isabelle Fajac; Christopher H Goss; Pavel Drevinek; Philip M Farrell; Anna M Gravelle; Trudy Havermans; Nicole Mayer-Hamblett; Nataliya Kashirskaya; Eitan Kerem; Joseph L Mathew; Edward F McKone; Lutz Naehrlich; Samya Z Nasr; Gabriela R Oates; Ciaran O'Neill; Ulrike Pypops; Karen S Raraigh; Steven M Rowe; Kevin W Southern; Sheila Sivam; Anne L Stephenson; Marco Zampoli; Felix Ratjen
Journal:  Lancet Respir Med       Date:  2019-09-27       Impact factor: 30.700

2.  Cystic fibrosis in Tuscany: evolution of newborn screening strategies over time to the present.

Authors:  Matteo Botti; Vito Terlizzi; Michela Francalanci; Daniela Dolce; Maria Chiara Cavicchi; Anna Silvia Neri; Valeria Galici; Gianfranco Mergni; Lucia Zavataro; Claudia Centrone; Filippo Festini; Giovanni Taccetti
Journal:  Ital J Pediatr       Date:  2021-01-06       Impact factor: 2.638

3.  V232D mutation in patients with cystic fibrosis: Not so rare, not so mild.

Authors:  Ana E Fernández-Lorenzo; Ana Moreno-Álvarez; Cristóbal Colon-Mejeras; Francisco Barros-Angueira; Alfonso Solar-Boga; Josep Sirvent-Gómez; María L Couce; Rosaura Leis
Journal:  Medicine (Baltimore)       Date:  2018-07       Impact factor: 1.889

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.