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.

 

It’s important for you to speak with a genetics professional prior to having carrier screening. Through some programs, a saliva sample can be collected at home and sent to a laboratory for analysis. Saliva testing does not include Tay-Sachs enzyme analysis, but may provide sequencing of multiple genes.

For more information, visit the Screening Centers page.

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