{Reference Type}: Journal Article
{Title}: [Expert consensus on the follow-up of newborn screening for neonatal genetic and metabolic diseases].
{Author}: Committee For Proficiency Testing Neonatal Genetic Metabolic Disease Screening Center National Health Commission Of China ;Ou M;Jiang J;Wang Z;
{Journal}: Zhonghua Yi Xue Yi Chuan Xue Za Zhi
{Volume}: 37
{Issue}: 4
{Year}: Apr 2020 10
暂无{DOI}: 10.3760/cma.j.issn.1003-9406.2020.04.002
{Abstract}: Follow-up is a crucial step for the screening of neonatal genetic and metabolic diseases, which can directly influence the detection, diagnosis, efficacy of treatment, as well as the quality of neonatal screening. In view of the lack of follow-up, full understanding, and inconsistent requirement between various agencies and personnel in China, there is an urgent need for standardization. The Committee for Proficiency Testing of the Neonatal Genetic Metabolic Disease Screening Center of the National Health Committee of China has organized the writing of expert consensus for follow-up of neonatal genetic and metabolic disease screening after thorough discussion, so as to guide the follow-up work and improve its quality.