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Essay text:
A baby with Tay-Sachs disease is born without the enzyme called Hexosaminidase A (Hex A). Hex A is one of the enzymes that clear out the fatty proteins, but without it the fatty proteins build up in the nerve cells in the brain. In reaction to the build up the baby's hearing, sight, movement and mental development is affected. A relentless deterioration of mental and physical abilities will occur.
Tay-Sachs disease is an autosomal recessive genetic condition. A baby will only receive the disease if both parents are carriers of the gene. When two parents, that are carriers, have a baby there is:
· 50% chance that their child will be a carrier, but will not have the disease
· 25% chance that their child will not be a carrier and not have the disease
· 25% chance that their child will have the disease
Below there is a picture illustration of the recessive pattern...
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