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 contribute actively to improving the quality of patients’ and their families’ life, both from a social and health point of view;
Information to release news and updates to families with affected persons, to sensitize the public opinion of the existence of this disease and of the related problems.