Overview
Screen4Care offers an innovative research approach to accelerate rare disease diagnosis based on genetic newborn screening and digital technologies. The project involves participation in genetic newborn screening and aims to shorten the path to rare disease diagnosis.
In the news
- How can NBS enable earlier intervention while ensuring its benefits are responsibly balanced? For Jan Kirschner from Universitätsklinikum Freiburg, realising the potential of NBS also means carefully considering the challenges it brings. 👇 #NewbornScreeningAwarenessMonth #NewbornScreening #Screen4Care #RareDiseases
- What role could NBS play in shaping the future of genomic medicine? For Alessandra Ferlini, Screen4Care Scientific Coordinator from Università degli Studi di Ferrara, the potential goes far beyond diagnosis 👇 #NewbornScreeningAwarenessMonth #NewbornScreening #Screen4Care #RareDiseases
- It’s September, which for us means one thing: Newborn Screening (NBS) Awareness Month is here! Throughout the month, we’ll be sharing voices from across the #Screen4Care team on where NBS stands today and where it could take us next. As a project committed to advancing NBS, raising awareness remains an important part of our mission, and we hope you’ll join the conversation. So make sure to follow along and stay tuned ✨ #RareDiseases #NewbornScreening
- Today, we join the global community in celebrating the International Day of Neonatal Screening! As a project committed to helping shape the future of #NewbornScreening, we are proud of the progress made together with our partners across Europe to enable faster diagnosis of rare diseases. We also celebrate the many projects, initiatives, and colleagues around the world who share this mission and are helping advance neonatal screening every day. 💙 Together, we are many. Together, we are building a future where every child has the
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