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Galactosemia / Galactose-1-phosphate uridylyltransferase deficiency / Galactosemic cataract / Inborn errors of carbohydrate metabolism / Medicine / Health


Medical Information Sheet GALACTOSEMIA What is galactosemia? Galactosemia is a rare hereditary disease that can lead to cirrhosis in infants, and early, devastating illness if not diagnosed quickly. This disease is cause
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Document Date: 2013-09-26 16:14:18

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City

Markham / /

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MedicalCondition

galactosemia and other forms / GALACTOSEMIA / Vomiting / rare hereditary disease / bacterial infections / disease / diarrhea / deficiency / illness / liver disease / cirrhosis / /

MedicalTreatment

blood transfusions / /

Organization

Canadian Liver Foundation National Office / /

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ProvinceOrState

Ontario / /

URL

www.liver.ca / /

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