Investigation of the effect of vitamin K1 prophylaxis on newborn screenings tests in newborns

BACKGROUND: Routine screening for hereditary disorders in newborns includes screening for treatable metabolic and endocrine disorders, such as biotidinase deficiency, galactosemia, maple syrup urine disease, hypothyroidism, and cystic fibrosis. Incorrect test results may be encountered due to the us...

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Detalles Bibliográficos
Autores principales: Caglayan, Murat, Gonel, Ataman, Tayman, Cuneyt, Cakir, Ufuk, Koyuncu, Ismail, Temiz, Ebru, Sert, Yasemin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Medical Biochemists of Serbia, Belgrade 2023
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560507/
https://www.ncbi.nlm.nih.gov/pubmed/37814616
http://dx.doi.org/10.5937/jomb0-40162

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560507/
https://www.ncbi.nlm.nih.gov/pubmed/37814616
http://dx.doi.org/10.5937/jomb0-40162

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