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新生儿原发性 T 细胞免疫缺陷的筛查:共识与争议。

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

机构信息

Department of Pediatrics, Medical College of Wisconsin and Children's Research Institute, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

出版信息

Expert Rev Clin Immunol. 2011 Nov;7(6):761-8. doi: 10.1586/eci.11.25.

DOI:10.1586/eci.11.25
PMID:22014017
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.

摘要

新生儿筛查以早期识别 T 细胞淋巴细胞减少症和严重联合免疫缺陷症,最近被建议作为所有州新生儿筛查计划的补充。本文将回顾支持使用这种新生儿筛查测试的证据,并概述全国实施的障碍,其中包括该测试的具体问题以及关于新生儿筛查的一般争议。

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Newborn Screening for Severe Combined Immunodeficiency.新生儿严重联合免疫缺陷病筛查。
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The respiratory presentation of severe combined immunodeficiency in two Mennonite children at a tertiary centre highlighting the importance of recognizing this pediatric emergency.两家系严重联合免疫缺陷在一家三级中心的呼吸表现,突出了认识这种儿科急症的重要性。
Can Respir J. 2014 Jan-Feb;21(1):17-9. doi: 10.1155/2014/404506. Epub 2013 Nov 28.