Leading the worldwide fight to treat and cure
Tay-Sachs, Canavan, GM1 and Sandhoff diseases

  • 1

Latest News

  • 1
  • 2

 

NTSAD leads the worldwide fight to treat and cure
Tay-Sachs, Canavan, GM1, and Sandhoff diseases
by driving research, forging collaboration, and fostering community.

Supporting families is the center of everything we do.

Join us, learn more, and support our cause.

 

No. Carriers do not express the symptoms of the disease. You need two mutated copies of a particular gene, one inherited from each parent, to develop an autosomal recessive disease.

For more information about autosomal recessive inheritance, visit the About Inheritance page.

Login