Sandhoff disease
Sandhoff disease is a type of GM2 gangliosidosis, characterised by low hexosaminidase A and B levels in leukocytes.
It is similar to Tay-Sachs disease and presents with a progressive loss of motor and language milestones from a young age.
It is usually fatal before the third year of life.
Create an account to add page annotations
Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.