What we do

The AT National Association is engaged in supporting:

Scientific research to get to a treatment for this rare genetic disease that causes a severe disability and early death;

Prevention to promote an early and reliable diagnosis;

Therapy to request structures that effectively contribute to the improvement of the quality of life of the patients and their families, both from a social and a healthcare standpoint;

Information to spead news and updates among afflicted families and the public opinion, to raise awareness of the existence of this disease and the related problems.