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Galactose-1-phosphate uridylyltransferase deficiency
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1	Galactosaemia fact sheet Dr Janice Fletcher, MD, FRACP, BSc Clinical Geneticist (HGSA), FRCPA Metabolic Clinic Women’s and Children’s Hospital 72 King William Road Add to Reading List Source URL: www.wch.sa.gov.au Language: English - Date: 2009-03-30 00:40:37 Chemistry Medicine Galactose Milk Lactose Galactose-1-phosphate uridylyltransferase deficiency Enzyme Infant Galactokinase deficiency Inborn errors of carbohydrate metabolism Galactosemia Health
2	Galactosemia Testing Algorithm ■ ■ ■ Clinical suspicion of classic galactosemia Add to Reading List Source URL: www.mayomedicallaboratories.com Language: English - Date: 2014-10-13 12:57:15 Galactosemia Galactose-1-phosphate uridylyltransferase deficiency Biology Medicine Galactokinase Galactose UDP-glucose 4-epimerase Galactosemic cataract Galactokinase deficiency Inborn errors of carbohydrate metabolism Health Galactose—1-phosphate uridylyltransferase
3	May[removed]Volume 30 Number 5 Feature Add to Reading List Source URL: www.mayomedicallaboratories.com Language: English - Date: 2010-04-29 15:46:04 Biology Galactosemia Galactose-1-phosphate uridylyltransferase deficiency Galactose—1-phosphate uridylyltransferase Galactokinase deficiency Galactokinase Galactose UDP-glucose 4-epimerase Galactosemic cataract Inborn errors of carbohydrate metabolism Health Medicine
4	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 Add to Reading List Source URL: liver.ca Language: English - Date: 2013-09-26 16:14:18 Galactosemia Galactose-1-phosphate uridylyltransferase deficiency Galactosemic cataract Inborn errors of carbohydrate metabolism Medicine Health
5	Galactosemia Carmen Lozzio, MD University of Tennessee Developmental and Genetics Center Knoxville, Tennessee Outcome without screening: Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2006-10-30 12:05:26 Galactosemia Biology Galactose-1-phosphate uridylyltransferase deficiency Galactose—1-phosphate uridylyltransferase Galactosemic cataract Galactokinase Galactitol Galactose Newborn screening Inborn errors of carbohydrate metabolism Health Medicine
6	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 milk sugar (e.g., da Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:49:16 Biology Galactosemia Galactose-1-phosphate uridylyltransferase deficiency Galactosemic cataract Galactose—1-phosphate uridylyltransferase Inborn errors of carbohydrate metabolism Medicine Health
7	Parents’ Guide to Galactosemia Part 2: Your Child Six Months and Older To Parents This booklet was written for parents of children with Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-10-06 16:45:51 Health Galactosemia Galactose-1-phosphate uridylyltransferase deficiency Galactose—1-phosphate uridylyltransferase Inborn errors of carbohydrate metabolism Food and drink Biology
8	Galactosemia Galactosemia is an inherited disorder of galactose metabolism. The main dietary source of galactose is lactose, which is found in milk. Clinical features of Galactosemia are failure to thrive (most common in Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:37:56 Medicine Biology Galactose-1-phosphate uridylyltransferase deficiency Galactose Beutler test Lactose Milk Galactosemic cataract Inborn errors of carbohydrate metabolism Galactosemia Health
9	NEWBORN SCREENING FACT SHEET Galactosemia What is it? A person who has galactosemia cannot break down galactose (a sugar found in milk and milk products). The body breaks down galactose into Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:32:03 Medicine Newborn screening Galactose Milk Human breast milk Galactosemic cataract Galactose-1-phosphate uridylyltransferase deficiency Inborn errors of carbohydrate metabolism Health Galactosemia
10	Newborn Screening Annual Report SFY12 Newborn Screening in Arkansas SFY12 Report of Results from July 1, 2011 – June 30, 2012 Child and Adolescent Health Section Add to Reading List Source URL: www.healthy.arkansas.gov Language: English - Date: 2014-07-17 12:11:10 Rare diseases Newborn screening Galactosemia Screening Congenital adrenal hyperplasia Galactose-1-phosphate uridylyltransferase deficiency Biotinidase deficiency Isovaleric acidemia Phenylketonuria Health Medicine Pediatrics