Galactosemia (G) is due to either partial or complete deficiency of the enzyme galactose-1-phosphate uridyl transferase (Ts). In females with G, there is a high incidence of premature ovarian failure.

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) is a ...

A 41-year-old woman with congenital glucose-galactose malabsorption (CGGM) was hospitalised for hypoglycaemia, and subsequent evaluation confirmed an insulinoma. Surgical resection was successful, and ...