In recognition of of National Rare Disease Day we would like to share The Faces of TANGO2 – a rare genetic disorder.
A disease may be rare, but hope should not be.
The TANGO2 Research Foundation would like to extend a special thanks to the following companies who have supported us through their matching gift programs. Their generous support has raised over $23K USD for the foundationRead more
When a new disease such as TANGO2 is discovered, there is a lot to learn. Many of the physicians caring for children with TANGO2 have never seen or managed this disease. The best way toRead more
On Wednesday, June 19th through Thursday June 20th, patients, families, doctors and other professionals will meet in Houston TX to discuss TANGO2 disease and how to best move forward with research around this rare andRead more
The Charles Dickens holiday classic, a Christmas Carol, was the backdrop for a TANGO2 Research Foundation fundraiser held on November 30, 2018 in Turin, Italy. The show was performed by Varallo’s Company, a local non-profitRead more
Davide, a friend of Rashmi and Giorgio, organized his farewell party in support of TANGO2 research. Thanks to his idea and the participation of many close friends, he raised nearly $2K dollars for the Foundation.Read more