Galactosemia
Inside the condition centers at ThirdAge.com you can learn more about all conditions, including Galactosemia. Research the condition by topics such as causes, symptoms, diagnosis, complications, and more. Learn how to take action with information on Galactosemia treatment options, prevention methods, support groups, and more. Select a topic below for more information.
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What is Galactosemia?
Classic galactosemia is an inherited disease. Due to a defective gene, there is a deficiency of the enzyme galactose-1-phosphate uridyltransferase. This enzyme is necessary for the conversion of galactose to glucose. Galactose is a simple sugar found in milk products. (The main sugar in milk is called lactose. It is made up of two simple sugars: galactose and glucose.) Glucose is the usable form of sugar in the human body.
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 Risk Factors Are you at risk of getting Galactosemia? Inside you'll find known risk factors for the condition. |
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 Diagnosis How will your doctor diagnose you with this condition? Learn about the tests, process, and more. |
 Complications Can this condition lead to other health problems? Learn more about the known complications. |
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 Screening Learn more about the specific tests or exams given by your doctor to screen for Galactosemia. |
 Medications What medications offer relief or help with this condition? Are there side effects? Risks? Learn more. |
 Prevention How can you prevent Galactosemia? Read what the medical community suggests for prevention methods. |
 Care Learn more about the day to day care of this condition. Changes to your activity, diet, exercise, and more. |
 Find a Doctor Do you need to contact a doctor about Galactosemia? Select a location to find a specialist in your area. |
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