Answer:
A. Ingestion ->Digestion ->Egestion
Tay-Sachs disease is caused by mutations in the HEXA gene and inheritance is autosomal recessive . The HEXA gene gives the body instructions to make part of the beta-hexosaminidase A enzyme, which is needed to break down a substance called GM2 ganglioside.
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<span>Pancreas. The pancreas does so by having beta cells that secrete a certain amount of insulin after consumption of food. There are then delta cells that regulate the beta cells, and then gamma cells that in turn regulate the delta cells.</span>
