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.
Angelique and Jeffrey van der Haar of Delft, Netherlands wanted to come to the TANGO2 Family Conference in Houston this past June with their son Liam, who has TANGO2, and his sister Alyssa. At theRead more
The very first TANGO2 Family Conference, hosted by the Baylor College of Medicine and the TANGO2 Research Foundation at The Westin Houston, Memorial City is about to get underway. Families, doctors and researchers are beginningRead more
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