Combined genetic screening and traditional newborn screening to improve the screening efficiency of congenital hypothyroidism
BACKGROUND: Congenital hypothyroidism (CH) is an neonatal endocrine disorder. Traditional newborn screening is the mainstream method of CH screening, so as to ensure the early detection and treatment of CH. This method is limited as it has high rates of false positives and negatives. Genetic screeni...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213735/ https://www.ncbi.nlm.nih.gov/pubmed/37252044 http://dx.doi.org/10.3389/fped.2023.1185802 |