Using the terms above correctly to show that you understand how genetics, protein synthesis, genetic
material and mutations can cause a disease like tay sachs syndrome explain in detail underlining your
terms as you go walk me through how a family with healthy genetics can wind up with a baby
that has
tay
sachs syndrome.

Tay-Sachs Disease is a genetic disorder caused by mutations in the HEXA gene, leading to fat accumulation in nerve cells and neurological issues. The disease follows autosomal recessive inheritance patterns.

Explanation:

Tay-Sachs Disease is a genetic disorder resulting from mutations in the HEXA gene on chromosome 15. This gene encodes an enzyme crucial for breaking down fats in nerve cells. Inheritance follows autosomal recessive patterns, meaning both parents must pass on a defective gene for the child to develop the disease.

Learn more about Genetic Disorders here:

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