• Tay-Sachs Disease



    Tay-Sachs disease (TSD) is a genetic disorder. It occurs when a fatty substance builds up in the brain. This causes progressive destruction of the brain. There are 3 forms:
    • Infantile-onset—usually fatal before 5 years of age
    • Juvenile-onset—usually fatal in late childhood or adolescence
    • Adult-onset—may survive up to 60 years of age


    TSD is caused by the absence of an enzyme. This enzyme is needed to break down a fatty substance called ganglioside (GM2). As a result, GM2 builds up. The build up in the brain causes damage.
    TSD occurs when both parents 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.
    Genetic Material
    Chromosome DNA
    Copyright © Nucleus Medical Media, Inc.

    Risk Factors

    Having parents who are carriers of the TSD gene is the most common risk factor.
    TSD is found in specific ethnic groups:
    • Those of Eastern European (Ashkenazi) Jewish descent
    • French Canadians living in eastern Quebec and New England
    • Select Cajun populations in Louisiana
    • Non-Amish Pennsylvania Dutch


    Babies with TSD may seem to develop normally until about 4-5 months of age when 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
    • Muscular difficulties such as spastic muscles, weakness, or paralysis
    • Intellectual disability
    • Seizures
    In some cases, the symptoms do not begin until age 2-5 years old. The condition progresses slowly. Symptoms may include:
    • Loss of the ability to speak
    • Developmental delay and intellectual disability
    • Loss of bowel control
    • Sleep problems
    • Movement disorder, such as difficulty walking and muscle weakness
    • Tremor
    • Slurred speech
    • Psychiatric problems
    • Loss of vision
    • Spasticity and 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 child's bodily fluids may be tested. This can be done with blood tests.


    There is presently no treatment for TSD. Treatment is aimed at managing symptoms.


    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 also available.


    Genetic Alliance http://www.geneticalliance.org

    National Tay-Sachs and Allied Diseases Association, Inc. http://www.ntsad.org


    About Kids Health—The Hospital for Sick Children http://www.aboutkidshealth.ca

    Caring for Kids—The Canadian Paediatric Society http://www.caringforkids.cps.ca


    Fernandes Filho JA, Shapiro BE. Tay-Sachs disease. Arch Neurol. 2004;61(9):1466-1468.

    Tay-Sachs disease. EBSCO DynaMed website. Available at: http://www.ebscohost.com/dynamed. Updated January 16, 2012. Accessed August 9, 2013.

    NINDS Tay-Sachs disease information page. National Institute of Neurological Disorders and Stroke website. Available at: http://www.ninds.nih.gov/disorders/taysachs/taysachs.htm. Updated October 6, 2011. Accessed August 9, 2013.

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