"Tay-Sachs disease is a lysosomal storage disease, which together with Sandhoff syndrome and AB variant comprise the GM2 gangliosidoses."
Expected headings
"At 3 to 6 months"
"At 6 to 10 months"
"10 months and older"
"Screening"
"As a child with Tay-Sachs grows older, he or she may become blind, intellectual impaired, paralysed, and unresponsive to the environment. The child also may have seizures, difficulty swallowing, and difficulty breathing. Children with Tay-Sachs disease rarely live beyond 4 or 5 years of age 1-7."