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

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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.

 

Both parents need to be carriers for a child to be affected with an autosomal recessive disease like Tay-Sachs. However, there is a 50% chance with each pregnancy that your child will be a carrier (like you) and a 50% chance that your child will inherit two normal copies of the Tay-Sachs gene.

For a graphic explanation, please visit the About Inheritance page.

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