A world where every person with Argonaute syndrome can thrive. Founded 2021 by Nora Leonardi.
Accelerate treatment
Connect & support
Raise awareness
Every child thrives
| Name | AGO Alliance |
| Type | Swiss Association (Verein), Tax-Exempt |
| Founded | 2021 by Nora Leonardi |
| Address | c/o Nora Leonardi, 8008 Zürich (Seefeld) |
| Phone | +41 44 383 67 14 |
| D-U-N-S® | 480551786 |
| Website | argonautes.ngo |
| Focus | AGO1 & AGO2 Gene Mutations |
In 2020, Nora and Christoph Leonardi’s daughter was diagnosed with a rare gene mutation in AGO2. At the time, there was limited knowledge — and the available prognoses were severe.
In 2021, they founded the AGO Alliance to accelerate therapeutic development, connect families, and raise awareness for Argonaute Syndromes.
Rare neurodevelopmental disorders caused by mutations in the AGO1 and AGO2 genes. These conditions often receive insufficient attention from pharmaceutical companies.
“A world where every person with Argonaute syndrome can thrive.”
From a family’s journey to a global mission — accelerating treatments for rare Argonaute syndromes.
Finding and funding paths to treatment for AGO1 and AGO2 syndromes — filling the gap left by pharmaceutical companies for rare diseases.
Building a global community of families affected by Argonaute syndromes — sharing experiences, knowledge, and support.
Educating medical professionals and the public about these rare neurodevelopmental disorders to improve diagnosis and care.
Working to ensure rare disease patients receive the attention, resources, and treatments they deserve.
Effective Date: March 13, 2026
AGO Alliance (“we”) operates Piggy Adventure (the “App”). We comply with Swiss nDSG/FADP, EU GDPR, and applicable privacy laws.
AGO Alliance | D-U-N-S® 480551786 | c/o Nora Leonardi, 8008 Zürich | +41 44 383 67 14 | privacy@argonautes.ngo
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AGO Alliance | D-U-N-S® 480551786 | c/o Nora Leonardi, 8008 Zürich | +41 44 383 67 14 | privacy@argonautes.ngo