Tay-Sachs disease

Tay-Sachs is a genetic disease. It happens when Chromosome 15 has a genetic problem. The problem is caused by a defective HEXA gene. It is recessive, which means both parents must give the baby the defective gene for the baby to have Tay-Sachs. One in every twenty seven Jewish American has one defective gene and can give Tay-Sachs the defective gene to their child. The disease is very rare. It is most common in Jewish families. There is a blood test to see if a person has the Tay Sachs gene. This blood test has helped reduce the number of babies born with Tay-Sachs. In 1800’s, there were 60 new cases and in the 21st century there were 5.

Treatment for Tay-Sachs disease

The focus of treatment for Tay-Sachs disease is to control symptoms and make your child as comfortable as possible. There is no cure. It may be helpful to seek counseling or find support from others who are going through the same thing you are.

If you have late-onset Tay-Sachs disease (LOTS), treatment also focuses on controlling symptoms. The treatment you receive, such as medicine for depression, depends on the symptoms you have.

It may be overwhelming to learn that your child has Tay-Sachs. It's important that you care for yourself as well as your child. Talk to your doctor about:

Your concerns and the help you'll need for your child.
A support group in your area.
Family counseling to help each member cope with the disease.
As the disease gets worse, your child will need more care. Encourage your child to be as active as possible for as long as possible. Give your child your love and affection.