Answer: True
Explanation:
Tay-Sachs disease can be defined as an autosomal recessive disorder in which there is a mutation on the hexa gene on the chromosome number 15 which codes for the subunit of the enzyme hexosaminidase.
This gene is inherited from a parent in an autosomal recessive manner. It is a genetic order which leads to destruction of nerve cells in the brain.
There is a hearing loss, seizures, and inability to move. These are some of the symptoms of Tay-sachs disease.
