Gene Typing Tay-Sachs
Tay-Sachs disease is an inherited metabolic disease of lysosomal lipid metabolism, and it is caused by the mutation of genes encoding the HEXB gene. It is a very severe genetic disorder which occurs in children in most cases and results in progressive destruction of the nervous system of the affected individual (Walker, 2007). The factors that cause the occurrence of the diseases is the absence of the hexosaminidase-A (HEX-A) enzyme that is very critical to have in the human genetic system. The lack of the HEX-A enzyme causes the accumulation of a fatty substance known as GM2 ganglioside in ...
