The Changing Face of Cystic Fibrosis and Its Implications for Screening

被引:11
|
作者
Naehrlich, Lutz [1 ]
机构
[1] Justus Liebig Univ Giessen, Dept Pediat, D-35392 Giessen, Germany
关键词
cystic fibrosis; newborn screening; diagnosis; therapy; prognosis; IVACAFTOR; PANCREAS; DISEASE; GUIDELINES; EFFICACY; THERAPY; SAFETY; SWEAT; ECFS; GENE;
D O I
10.3390/ijns6030054
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Early diagnosis, multidisciplinary care, and optimized and preventive treatments have changed the face of cystic fibrosis. Life expectancy has been expanded in the last decades. Formerly a pediatric disease, cystic fibrosis has reached adulthood. Mutation-specific treatments will expand treatment options and give hope for further improvement of quality of life and life expectancy. Newborn screening for CF fits perfectly into these care structures and offers the possibility of preventive treatment even before symptoms occur. Especially in countries without screening, newborn screening will fulfill that promise only with increased awareness and new care structures.
引用
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页数:8
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