The galactose then cannot be broken down and enters the bloodstream. Galactosemia can develop in any of numerous ways, and affects every individual differently. Some people develop galactosemia through birth, while others develop it later in life. There are some rare genetic disorders, too. While galactosemia is a rare condition today, for many years it was common among infants and children with diarrhea. It can affect anyone over the age of 6. It does not affect adults. What is the Diagnosis Galactosemia is an acquired disorder of metabolism, not a disease. The diagnosis is based on laboratory tests that measure levels of galactose in the blood. They may suggest that there may be a problem with the digestive system. Treatment There is no cure for galactosemia. There is no treatment to prevent it, except to avoid exposure to galactose (milk, sugar). There are no medications that will treat galactosemia, or prevent it. However, doctors can help control it by educating their patients and the patient's family.
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Galactosemia What is Galactosemia? Galactosemia is an inherited condition that affects the way a person's body breaks down galactose. When a person eats or drinks a product that contains lactose or
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