NTSAD provides family services, research, and education for
Tay-Sachs, GM-1, Sandhoff, Canavan and allied diseases.
Join our cause to wipe out these genetic diseases.
The severity of a Lysosomal storage disorder depends on the amount of enzyme activity that is present, and where in the body the substrate (debris) is accumulating. If some enzyme activity is present, symptoms usually begin later on (as in juvenile or adult onset version of the diseases.) The most severe disorders are where the debris builds up in the central nervous system, such as in Tay Sachs, Sandhoff and GM-1.