Trisomy 21 Research Society (T21RS) is the first international non-profit scientific organization of researchers studying Down syndrome. T21RS was founded to promote basic and applied research on Down syndrome, stimulate translational research and apply new scientific knowledge to improve the quality of life for people with Down Syndrome.
News
LUMIND – myDSC Webinar: Dermatology and Down Syndrome
T21RS Webinar – Dec 10, 2024
London-Cambridge Down syndrome Seminar Series Virtual/Hybrid 2024-2025
T21RS Webinar – Oct 29, 2024
Nominations for the Chair of the Program Committee
Nomination for the Chair(s) of the Clinical Research Committee
T21RS Members Initiatives 2024
Contribute DS article: Special Issue of Brain Sciences
6th T21RS International Conference – Colorado 2026
New Neuropathology Working Group
COVID-19 vaccinations are safe to use in people with Down syndrome
T21RS endorses the ALBA Declaration on Equity and Inclusion
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