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.

If you've ever paid attention to food labels, you've likely noticed that many ingredients, such as high fructose corn syrup, end with the suffix "ose." This is because this suffix is one way ...

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. ...

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 ...

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 ...

How often should you test your glucose and A1C? How do food, sleep and exercise affect blood sugar? Here’s what to know. Credit...Illustration by Andrei Cojocaru; Photos by Getty Supported by By ...

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 ...

I was worried that whatever I chose to eat would cause the new app on my phone to record a spike in my glucose levels that would count against the number I was allowed that day – and I was ...