Tay-Sachs Disease

Tay-Sachs-Disease

Tay-Sachs disease is a rare, inherited disorder. It causes too much of a fatty substance to build up in tissues and nerve cells of the brain. This buildup destroys the nerve cells, causing mental and physical problems.

Tay-Sachs disease is a rare, inherited disorder. It causes too much of a fatty substance to build up in tissues and nerve cells of the brain. This buildup destroys the nerve cells, causing mental and physical problems. Infants with Tay-Sachs disease appear to develop normally for the first few months of life. Then, as nerve cells become distended with fatty material, mental and physical abilities deteriorate. The child becomes blind, deaf, and unable to swallow. Muscles begin to atrophy and paralysis sets in. Even with the best of care, children with Tay-Sachs disease usually die by age 4.
Tay-Sachs is most common in Eastern European Ashkenazi Jews. A blood test can determine if you carry or have the disease. There is no cure. Medicines and good nutrition can help some symptoms. Some children need feeding tubes.

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2 thoughts on “Tay-Sachs Disease

  1. Vikram says:

    Need more information, if there is no cure then what does this medicine does ? Its just make sure to avoid condition worsening ? and as per your description child cant live more than 4 years of age

      • Premilife Customer Care says:

        Dear Vikram
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        We have answered your question in a personal email sent to you.
        We hope you found our answer sufficient and that it provided you with the information you were looking for.
        If you have further questions, please feel free contacting us using the Contact Premilife page. We will be happy to assist.
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