Increase understanding of the features of AGO1 and AGO2 and what this means for children with these diseases
Help scientists understand the real-life challenges that patients face
Encourage research ideas and collaborations
Unite patient families to share experiences and support each other
Share learnings to raise awareness and engage with the AGO community
Our 1st Argonaute Syndromes Conference where researchers and patient families from around the world came together was a resounding success. It was a weekend full of emotions, learning and sharing. A huge thanks to everyone who contributed - in person or virtually.Syndrome & conference highlights
Read conference report (7 min)
Our event took place as a satellite of the 1st conference on Argonaute proteins. We are very grateful for this collaboration and look forward to joining forces again in 2024.
This event wouldn't have been possible without the support of the EU's European Joint Programme on Rare Disease (EJPRD) and Costello Medical.
To access conference recordings, please email us.