Galactosemia :: essays research papers

GalactosemiaGalactosemia is a genetically inherited metabolic disorder. This disorder leaves the disable with a partial or complete lack of the enzyme Galactose 1 Phosphate Uridyl Transferase (GALT). This enzyme is found in the bloodstream and it is used for breaking calibrate the sugar galactose. This disorder comes in both different variations. Though there is more than one(a) type, it is still rare, having scarcely 1 in 80,000 births universe affected by the disorder.Classic Galactosemia is the first and more common found of the disorder. This is the form when the affected has a complete loss of the enzyme. Both parents moldiness contribute a galactosemic gene for a child to receive this really deadly form of the disorder. Because the body has none of the enzyme needed to turn galactose into glucose an accumulation occurs that is like a poison and is highly fatal. Classic Galactosemia is treatable finished a strict victuals of absolutely no lactose or galactose. Some common foods containing these are dairy products, legumes, breast milk, and many differentwise foods. A test for galactosemia is done at the time of birth with other tests. If left untreated 75% of infants will die. Some effects of having clear galactosemia include an enlarged liver, kidney failure, cataract, and brain damage.Duarte Galactosemia is the second form. This form is when there is only a partial loss of the enzyme. The activity is usually 25%-50% that of a normal child. A child throne get this form of galactosemia by inheriting a classic galactosemia gene from one parent and a duarte gene from the other. Much like classic galactosemia, duarte is found through a test done soon after birth. A strict diet is not needed for this form of the disorder. Instead a diet, it is recommended that lactose be slowly introduced untill normal consumption is accepted by the body. Because the affected can still process the foods, just not as well as a fully functional body.A person wi th no galactosemia receives two normal genes for production of the GALT enzyme in the bloodstream. This persons genotype is N/N and they control normal fully functioning enzyme activity. A carrier of classic galactosemia inheriets one affected gene and one non, this persons genotype is G/N. This person has slight than normal enzyme activity, but nothing that requires a diet or medical exam treatment. A classic galactosemic has two classic galactosemia genes.