Expert consensus on the follow-up of newborn screening for neonatal genetic and metabolic diseases / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
;
(6): 367-372, 2020.
Article
in Chinese
| WPRIM
| ID: wpr-828322
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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
China
/
Follow-Up Studies
/
Neonatal Screening
/
Consensus
/
Diagnosis
/
Genetics
/
Genetic Diseases, Inborn
/
Metabolic Diseases
Type of study:
Diagnostic study
/
Practice guideline
/
Observational study
/
Prognostic study
/
Qualitative research
/
Screening study
Limits:
Humans
/
Infant, Newborn
Country/Region as subject:
Asia
Language:
Chinese
Journal:
Chinese Journal of Medical Genetics
Year:
2020
Type:
Article
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