Glucose-galactose malabsorption (GGM) is a rare inherited metabolic disorder that prevents the body from absorbing two simple sugars: glucose and galactose. Glucose-galactose malabsorption (GGM ...

Glucose-galactose malabsorption (GGM) is a rare metabolic condition. It occurs when a genetic variation makes the body unable to properly absorb the simple sugars glucose and galactose.

THREE naturally occurring aldohexoses—glucose, mannose and galactose—can readily be differentiated by the following method. Add 2 mgm. of the unknown sugar material to a solution of ...

Lactase is encoded by a single gene (LCT) of approximately 50 kb located on chromosome 2. The gene has 17 exons and codes for an mRNA molecule which has 6274 bases with 1927 amino acid residues. ...

Galactosemia is a rare genetic disorder where galactose (a by-product of lactose digestion) fails to convert to glucose. Lactose is one of the main carbohydrate components present in milk.

If you’re a carrier, it doesn’t mean you have to avoid galactose. But it means you can pass galactosemia along to your children if your partner is also a carrier. If your newborn has classic ...

Lactose, or milk sugar, is a disaccharide made of two simple sugars – glucose and galactose – in a 1:1 ratio. It's found in mammals' milk and produced naturally to provide nutrition to ...

A home blood glucose test can be a safe and affordable way to check for diabetes before symptoms appear. The test involves dropping a small amount of blood onto a testing strip and reading the ...

It is the smallest building block of all sugars. There are three types of monosaccharides: glucose, fructose, and galactose. When two monosaccharides bond, they create a larger sugar compound call ...

This is the conclusion of a pair of studies by research teams from the U.S. and Ireland, respectively, which analyzed the impact of various forms of glucose-lowering drugs. These included GLP-1 ...