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What is Tay Sach’s disease?

Tay-Sachs disease is a fatal genetic lipid storage disorder in which harmful quantities of a fatty substance called ganglioside! Any Suggestions here?


  1. Manuela Reply:

    How to Prevent Tay-Sachs Disease. Tay-Sachs Disease is a fatal illness that can tear a family apart. Even under the best circumstances and care, most children Source:

  2. William Reply:

    Tay-Sachs disease is an uncommon disorder that is transmitted from parents to child. In the most ordinary form, a baby of about 6 months old will begin to demonstrate its symptoms. Find out more details here

  3. Patty Reply:

    Both mom and dad must be carriers of the tay sach gene in order to pass it along to their children. It is caused by a mutation on chromosome 15. Source:

  4. Hyun Reply:

    The Tay Sachs disease is not very common at all. It shows up very rarely in the general population. The disease shows up most often in people who are of the Ashkenazi Jewish heritage. Source:

  5. Shenika Reply:

    Tay Sachs is a fatal hereditary disease found most often if families of ceratin Jewish and Mediterranean decents. It is recessive, so both parents must carry the gene. Children with Tay Sachs rarely live past 1 year. Source:

  6. Shiela Reply:

    What is Tay-sachs Disease? This is the answer i got off the internet: Tay-Sachs is a hereditary disorder of lipid metabolism occurring most frequently in individuals of Jewish

  7. Martin Reply:

    genotype:TT,2Tt,ttphenotype: 1:3%=25%

  8. Loralee Reply:

    Tay-Sachs disease ( ) n. A hereditary disease that affects young children almost exclusively of eastern European Jewish descent, in which an enzyme.

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