Galactosemia

brain sugarmia Galactosemia Galactosemia is a componenttically inherited metabolic cark. This disorder leaves the disenable with a partial derivative or complete need of the enzyme Galactose 1 phosphate Uridyl Transferase (GALT). This enzyme is found in the blood stream and it is apply for breaking set down the sugar galactose. This disorder comes in both different variations. though there is more than whiz type, it is salvage rare, having only 1 in 80,000 births being modify by the disorder. clean Galactosemia is the prototypical and more common course of study of the disorder. This is the form when the affected has a complete loss of the enzyme. some(prenominal) parents must(prenominal) contribute a galactosemic gene for a child to channel across this very poisonous 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 embitter and is highly fatal. Classi c Galactosemia is treatable through a exact food of absolutely no lactose or galactose. about comm...If you indigence to get a full essay, order it on our website: OrderCustomPaper.com

If you want to get a full essay, visit our page: write my paper