| Literature DB >> 32219815 |
Mingcai Ou, Jianhui Jiang, Zhiguo Wang.
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.Year: 2020 PMID: 32219815 DOI: 10.3760/cma.j.issn.1003-9406.2020.04.002
Source DB: PubMed Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi ISSN: 1003-9406