Tay-Sachs disease (TSD) is a fatal genetic disorder. It occurs when a fatty substance builds up in the brain. This causes progressive destruction of the brain. There are three forms:
- Infantile-onset
- Juvenile-onset
- Adult-onset
Given the best of care, all children with the infantile form die by the age of five.
TSD is caused by the absence of an enzyme. This enzyme is needed to break down a fatty substance called GM2. As a result, GM2 builds up. The build up in the brain causes damage.
TSD occurs when both parent pass on the faulty genes. A person can have just one copy of the faulty gene. In this case, there are no symptoms. The person is called a carrier.
Factors that increase your chance for TSD include:
- Having parents who are carriers of the TSD gene
- Race: Eastern European (Ashkenazi) Jewish descent
- TSD is also frequently found in French Canadian and Cajun populations
Babies with TSD may seem to develop normally until about 4 to 5 months of age. There is then an arrest of development. Symptoms begin to occur. Symptoms may include:
- Floppy body position
- Shrill cry
- Decreased eye contact
- Increased startle reaction
- Loss of motor skills
- Enlarged head
- Vision loss or blindness
- Deafness
- Difficulty swallowing
- Slurred speech (juvenile-onset form)
-
Muscular difficulties, such as:
- Spastic muscles
- Weakness or paralysis
- Mental retardation
- Seizures
The doctor will ask about your child's symptoms and medical history. A physical exam will be done. The doctor may examine your child's eyes to look for a cherry red spot on the retina. Your doctor may also order:
- Blood test—to measure hexosaminidase A activity
There is presently no treatment for TSD. However, research is ongoing.
There are no known ways to prevent Tay-Sachs disease. If you are a carrier of the gene that causes TSD, you can talk to a genetic counselor before deciding to have children. Prenatal testing during the first trimester is available.
Last reviewed September 2009
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