Project: European network on Noonan syndrome and related disorders
RASopathies constitute a family of rare diseases affecting development and growth. These disorders include Noonan syndrome and an increasing number of clinically related conditions sharing dysregulation of RAS signaling as common pathogenetic mechanism. Major features include reduced growth, congenital heart disease, hypertrophic cardiomyopathy, cognitive deficits, facial dysmorphism, skeletal and hematologic anomalies, and variable predisposition to certain malignancies. Most of these disorders are genetically heterogeneous, and the partners of this Consortium
| Acronym | NSEuroNet |
| Duration | 01/01/2016 - 01/12/2018 |
| Project Topic | 7th JOINT CALL FOR EUROPEAN RESEARCH PROJECTS ON RARE DISEASES (JTC 2015) |
| Network | E-Rare-3 |
| Call | E-Rare-3 JTC 2015 |
Project partner
| Number | Name | Role | Country |
|---|---|---|---|
| 1 | Istituto Superiore di Sanità | Coordinator | Italy |
| 2 | Otto-von-Guericke University Magdeburg | Partner | Germany |
| 3 | Heinrich-Heine University Düsseldorf | Partner | Germany |
| 4 | Koninklijke Nederlandse Akademie van Wetenschappen | Partner | Netherlands |