Sandhoff Disease

The clinical course of Sandhoff disease is almost identical to that of Tay-Sachs disease except that there may be some extra neurological involvement such as organomegaly and skeletal involvement in the former.

Enzyme Test: b-hexosaminidase (total) is measured for diagnosis of this disease.

Back to Lysosomal Storage Disorders Index

Back to Alphabetical List of Assays Available


Web site by Paul Littlefield