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.