Towards Achieving Equity and Innovation in Newborn Screening across Europe

Towards Achieving Equity and Innovation in Newborn Screening across Europe

Although individual rare disorders are uncommon, it is estimated that, together, 6000+ known rare diseases affect more than 30 million people in Europe, and present a substantial public health burden. Together with the psychosocial burden on affected families, rare disorders frequently, if untreated...

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Bibliographic Details
Main Authors: Jaka Sikonja, Urh Groselj, Maurizio Scarpa, Giancarlo la Marca, David Cheillan, Stefan Kölker, Rolf H. Zetterström, Viktor Kožich, Yann Le Cam, Gulcin Gumus, Valentina Bottarelli, Mirjam van der Burg, Eugenie Dekkers, Tadej Battelino, Johan Prevot, Peter C. J. I. Schielen, James R. Bonham
Format: Article
Language:English
Published: MDPI AG 2022-05-01
Series:International Journal of Neonatal Screening
Subjects:
newborn screening
NBS
rare diseases
access inequality
Europe
Slovenia
Online Access:https://www.mdpi.com/2409-515X/8/2/31

Internet

https://www.mdpi.com/2409-515X/8/2/31

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