Cystic Fibrosis Carrier Screening

被引：16
|
作者：
Massie, John [1 ,2 ,3 ]
Delatycki, Martin B. [2 ,3 ]
机构：
[1] Royal Childrens Hosp, Dept Resp Med, Parkville, Vic 3052, Australia
[2] Murdoch Childrens Res Inst, Murdoch, WA, Australia
[3] Univ Melbourne, Dept Paediat, Melbourne, Vic 3010, Australia
来源：
PAEDIATRIC RESPIRATORY REVIEWS | 2013年 / 14卷 / 04期
关键词：
Cystic fibrosis; Carrier screening; PARENTAL ATTITUDES; POPULATION; PROGRAM; DIAGNOSIS; PREVALENCE; STRATEGIES; CHILDREN; VICTORIA; OUTCOMES; DISEASE;
D O I：
10.1016/j.prrv.2012.12.002
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Carrier screening for cystic fibrosis (CF) has been available since the early 1990s, yet there are few programs, and none funded as part of a national health care strategy. The aim of this paper is to provide a description of carrier screening for CF and examine the progress that has been made towards the establishment of universal population-based carrier screening programs. This is an evidence based commentary on population-based carrier screening for CF. Peak body recommendations were examined and existing programs for CF carrier screening are reviewed. The attitudes from the non-CF community, CF healthcare professionals and people with CF were studied. Data from health economic assessments is examined. The future of carrier screening for CF in the context of advancing genetic technologies and potentially curative therapies is considered. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码：270 / 275
页数：6
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