Neonatal screening for congenital hypothyroidism in an Italian Centre: a 5-years real-life retrospective study

INTRODUCTION: Congenital hypothyroidism is an endocrine disease with a significant incidence in the general population (1:2000–1:3000 newborns in Italy) and a different geographical distribution, partially explained by endemic iodine deficiency, genetic traits and autoimmune thyroid diseases. OBJECT...

Descripción completa

Detalles Bibliográficos
Autores principales: Maggio, Maria Cristina, Ragusa, Saveria Sabrina, Aronica, Tommaso Silvano, Granata, Orazia Maria, Gucciardino, Eleonora, Corsello, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097769/
https://www.ncbi.nlm.nih.gov/pubmed/33952334
http://dx.doi.org/10.1186/s13052-021-01053-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8097769/
https://www.ncbi.nlm.nih.gov/pubmed/33952334
http://dx.doi.org/10.1186/s13052-021-01053-0

Ejemplares similares