This delayed allergic reaction is called alpha-gal syndrome. While it’s commonly called the “red meat allergy ,” that ...

Glucose-galactose malabsorption (GGM) is a very rare inherited genetic condition, with only approximately 300 cases worldwide. GGM is also sometimes known as SGLT1 deficiency.

Galactosemia is a rare hereditary condition that impacts the body's capacity to process galactose, a sugar found in milk and dairy products, as well as some fruits and vegetables. Galactose is a ...

Glucose-galactose malabsorption describes a condition where a person cannot absorb these simple sugars. Due to a genetic alteration, a person does not produce the SGLT1 protein, which helps the ...

Lactose and galactose are taken out of their diet. Instead, they’re given soy-based formula and must avoid milk or milk byproducts. Your doctor will likely refer your child to a specialist.

Galactose is an essential component of galactoproteins and galactolipids. In GALT deficiency there is considerable endogenous production of galactose and production of UDP-galactose by reversal of the ...

Galactose metabolism disorders and more If the enzymes that convert galactose into Glucose are defective, galactose accumulates in the body. Slow, and in the term, we say that galactosemia has ...