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.
Artículo
en Chino
| 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.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
China
/
Estudios de Seguimiento
/
Tamizaje Neonatal
/
Consenso
/
Diagnóstico
/
Genética
/
Enfermedades Genéticas Congénitas
/
Enfermedades Metabólicas
Tipo de estudio:
Estudio diagnóstico
/
Guía de Práctica Clínica
/
Estudio observacional
/
Estudio pronóstico
/
Investigación cualitativa
/
Estudio de tamizaje
Límite:
Humanos
/
Recién Nacido
País/Región como asunto:
Asia
Idioma:
Chino
Revista:
Chinese Journal of Medical Genetics
Año:
2020
Tipo del documento:
Artículo
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