Two Associations, one shared fight: rare neurodevelopmental disorders
The Spanish association ASAGON and the French association Les Maux Dyrk d’Elouann are actively supporting research on AGO1 and DYRK1A syndromes.
Thanks to their donations, the team “Genetics and pathophysiology of neurodevelopmental Disorders,” led by Amélie Piton, will be able to advance the understanding of these complexgenetic syndromes and pave the way for new therapeutic approaches.
Learn how their support ismaking a real difference!
Two Committed Associations
ASAGON (Asociación de Síndromes AGO Navarra) is a Spanish association that supports families affected by syndromes related to the AGO1 gene.
This rare and still largely unknown condition affects around a hundred children worldwide. Thanks to its commitment, ASAGON has provided €10,000 in support of our work.
In France, the association Les Maux Dyrk d’Elouann is actively working to raise awareness of DYRK1A syndrome, inform the public, and support research.
It has contributed €3,000, helping to strengthen our research capacity.
Advancing Research, Opening Perspectives
These valuable contributions directly support our work, which aims to better understand how these genetic mutations impact brain development.
Our research focuses on three key areas:
Developing human brain cell models, including cerebral organoids derived from cells carrying these mutations
Analyzing cellular alterations (neurons, precursor cells...) and the effects on gene expression
Exploring new therapeutic avenues, with the goal of improving care for affected individuals over the long term
A huge thank you to ASAGON, Les Maux Dyrk d’Elouann, and to everyone who supports them.
Their commitment is a vital driving force for research progress and for opening concrete possibilities for families.
To learn more:
- ASAGON : https://asociacionsindromesago.org/
- Les Maux Dyrk d’Elouann : https://www.helloasso.com/associations/les-maux-dyrk-d-elouann