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Science
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Number of pages / Number of words: |
6 / 1593 |
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That allows the ganglioside GM2
to overly produce and go out of control. Tay-Sachs is recessive, and caused by the
mutations in both of the allelles belonging to Chromosome 15. During Tay-Sachs, Hex-
A is disfunctional and not working at all. With the absence of Hex A, the fatty substance
ganglioside GM2 accumulate abnormally inside of the brain...
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With the absence of Hex A, the fatty substance
ganglioside GM2 accumulate abnormally inside of the brain. It keeps reproducing, and
with so much of the substance, the brain cells are badly damaged. Tay-Sachs is inherited
from both parents. A blood test is the only way to find out if you have Tay-Sachs...
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