Galactosemia Galactosemia Galactosemia is an inborn error of metabolism. Because of energy barriers, essentially none of the chemical substance reactions that take place in living things could advance at any measurable rate without the presence of a catalyst. most(prenominal) catalysts in living things atomic number 18 enzymes that consider on their body social structure to be able to function. Their structure is determined by their cryptanalysis on DNA. Inborn errors of metabolism, equal the one seen in brain sugarmia, are caused by defective genes.
Galactosemia is an inherited metabolic dis regularize in which the t ransformation of galactose to glucose is blocked, allowing galactose to increase to toxic levels in the body (Chung 1997). Galactose epimerase, the enzyme in the liver that is required to set forth down galactose, is lacking(p) in galactosemia patients (Galactosemia 1995 and Wohlers, Christacos, and Harreman 1999). This enzyme works as a catalyst to fixedness up the breakdown of galactose. When there is a deficiency of this enzyme...If you pauperization to get a full essay, order it on our website: BestEssayCheap.com
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