Literature DB >> 32219815

[Expert consensus on the follow-up of newborn screening for neonatal genetic and metabolic diseases].

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


  2 in total

1.  Screening for neonatal inherited metabolic disorders by tandem mass spectrometry in Guangzhou.

Authors:  Chengfang Tang; Minyi Tan; Ting Xie; Fang Tang; Sichi Liu; Qingxiu Wei; Jilian Liu; Yonglan Huang
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2021-08-25

Review 2.  Recent research on inherited metabolic diseases in children.

Authors:  Yu-Jian Li; Xuan Kan
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2022-03-15
  2 in total

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