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Expanded newborn screening program in Slovenia using tandem mass spectrometry and confirmatory next generation sequencing genetic testing

机译:使用串联质谱和验证的下一代测序遗传检测,在斯洛文尼亚扩展新生儿筛查计划

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摘要

In the last two decades, the introduction of tandem mass spectrometry in clinical laboratories has enabled simultaneous testing of numerous acylcarnitines and amino acids from dried blood spots for detecting many aminoacidopathies, organic acidurias and fatty acid oxidation disorders. The expanded newborn screening was introduced in Slovenia in September 2018. Seventeen metabolic diseases have been added to the pre-existing screening panel for congenital hypothyroidism and phenylketonuria, and the newborn screening program was substantially reorganized and upgraded.
机译:在过去的二十年中,临床实验室中的串联质谱仪引入使得从干燥的血斑上同时测试许多氨基碱和氨基酸,以检测许多氨基酰胺化,有机酸核和脂肪酸氧化障碍。 2018年9月在斯洛文尼亚引入了扩展的新生儿筛查。将十七次代谢疾病添加到先天性甲状腺功能减速和苯丙酮尿中预先存在的筛查小组中,新生儿筛查计划基本上重组和升级。

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