Welcome to the International A-T Registry, the first ever registry dedicated to gathering clinical data on people with ataxia-telangiectasia and related conditions from around the globe.

By gathering clinical data on people with A-T and related conditions, the registry aims to improve our understanding of the conditions and how they develop, to help improve existing treatments and the develop new ones.

This project was established with funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (grant agreement n° 667946.)

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Total Patient Records

50
Female
47
Male
1
Undetermined