Current paediatric standard-of-care for galactosemia is a lactose-free diet. Image credit: Shutterstock / Photoongraphy. Nearly three months after an experimental treatment for classic galactosemia ...

Current paediatric standard-of-care for galactosemia is a galactose-free diet. Image credit: Shutterstock / Photoongraphy. Nearly three months after an experimental treatment for classic galactosemia ...

Classical galactosemia, a hereditary metabolic disease caused by the deficiency of galactose ... GALT(−) cell-specific effects in the absence of stressor revealed cell-model-dependent affection of ...

Glucose is used as a primary source of energy for the body. People with galactosemia may have no problem digesting lactose. But they have a shortage or absence of the liver enzyme GALT, which is ...

It’s easy to test for galactosemia. It’s also simple to treat once it’s diagnosed. And children who have it can live normal lives. Type I occurs in about 1 in every 30,000 to 60,000 people.

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.

Galactosemia is a rare genetic disorder that causes an inability to digest galactose, which is a breakdown product of lactose. Lactose is one of the main carbohydrates in milk. In the infant ...

Introduction:Galactosemia (GAL) is a genetic disorder that results in disturbances in galactose ... OPLS-DA models were evaluated using the fitness-of-model (R2Y) and predictive ability (Q2) values.

Since galactosemia is a rare inherited disorder its symptoms and treatment are widely unfamiliar to the public. It occurs in about 1 in 65,000 births in the United States. With this review, improve ...