English 
Spanish 
Russian 
German 
French 
Japanese 
Portuguese 
Hindi 开放获取期刊获得更多读者和引用
700 种期刊 和 15,000,000 名读者 每份期刊 获得 25,000 多名读者
抽象的
Newborn Screening for Cystic Fibrosis in Genetically Heterogeneous Populations
Alejandro Teper, Viviana Rodríguez
Cystic fibrosis is the most frequent autosomal recessive disease in Caucasians. Survival improves with the implementation of newborn screening programs that enable early detection and rapid initiation of treatment to reduce the effects of the disease. Not all available algorithms for newborn screening are suitable for all populations. IRT/PAP is the algorithm of choice in genetically heterogeneous populations.
免责声明: 此摘要通过人工智能工具翻译，尚未经过审核或验证。