Literature DB >> 22014017

Screening newborns for primary T-cell immunodeficiencies: consensus and controversy.

Deborah J Accetta Pedersen1, James Verbsky, John M Routes.   

Abstract

Newborn screening for early identification of T-cell lymphopenia and severe combined immunodeficiency has recently been recommended as an addition to the newborn screening programs in all states. This article will review the evidence supporting the use of this newborn screening test, and will outline the barriers to nationwide implementation, which include issues specific to this test and controversies regarding newborn screening in general.

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Year:  2011        PMID: 22014017     DOI: 10.1586/eci.11.25

Source DB:  PubMed          Journal:  Expert Rev Clin Immunol        ISSN: 1744-666X            Impact factor:   4.473


  4 in total

1.  Concurrent hearing and genetic screening in a general newborn population.

Authors:  Ling Guo; Jiale Xiang; Lei Sun; Xinyi Yan; Jingjing Yang; Haiyan Wu; Kejian Guo; Jiguang Peng; Xiaomei Xie; Ye Yin; Jian Wang; Huanming Yang; Jun Shen; Lijian Zhao; Zhiyu Peng
Journal:  Hum Genet       Date:  2020-01-30       Impact factor: 4.132

2.  The respiratory presentation of severe combined immunodeficiency in two Mennonite children at a tertiary centre highlighting the importance of recognizing this pediatric emergency.

Authors:  Simon Lam; Fotini Dimitriou Kavadas; Seemab Haider; Mary Elizabeth Noseworthy
Journal:  Can Respir J       Date:  2013-11-28       Impact factor: 2.409

Review 3.  The case for mandatory newborn screening for severe combined immunodeficiency (SCID).

Authors:  H B Gaspar; L Hammarström; N Mahlaoui; M Borte; S Borte
Journal:  J Clin Immunol       Date:  2014-04-02       Impact factor: 8.317

Review 4.  Newborn Screening for Severe Combined Immunodeficiency.

Authors:  John Routes; James Verbsky
Journal:  Curr Allergy Asthma Rep       Date:  2018-05-10       Impact factor: 4.806

  4 in total

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