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Galactose-1-phosphate uridylyltransferase deficiency
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31	MISSISSIPPI STATE DEPARTMENT OF HEALTH Newborn Screening Report[removed] AUTHORS AND CONTRIBUTORS Add to Reading List Source URL: www.msdh.state.ms.us Language: English - Date: 2011-11-18 10:10:08 Rare diseases Inborn errors of carbohydrate metabolism Epidemiology Newborn screening Galactosemia Screening Phenylketonuria Galactose-1-phosphate uridylyltransferase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics
32	GALACTOSEMIA Definition Galactosemia is an inherited disorder of carbohydrate metabolism, in which galactose cannot be converted to glucose because of the missing or deficient enzyme, galactose-1phosphate uridyl transfer Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:19 Galactosemia Biology Galactose-1-phosphate uridylyltransferase deficiency Galactose—1-phosphate uridylyltransferase Galactose Newborn screening Galactosemic cataract Carbohydrate metabolism Infant formula Inborn errors of carbohydrate metabolism Health Medicine
33	MISSISSIPPI STATE DEPARTMENT OF HEALTH Newborn Screening Report[removed] AUTHORS AND CONTRIBUTORS Add to Reading List Source URL: msdh.ms.gov Language: English - Date: 2011-11-18 10:10:08 Rare diseases Inborn errors of carbohydrate metabolism Epidemiology Newborn screening Galactosemia Screening Phenylketonuria Galactose-1-phosphate uridylyltransferase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Medicine Pediatrics
34	PARENT FACT SHEET DISORDER Galactosemia (GALT) CAUSE GALT is caused when the liver enzyme that helps the body break down galactose (a form of milk sugar) is either Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 12:33:44 Galactose Medicine Milk Galactose-1-phosphate uridylyltransferase deficiency Biology Galactosemic cataract Inborn errors of carbohydrate metabolism Galactosemia Health
35	Disease Name Galactosemia Acronym Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 19:34:47 Galactosemia Galactosemic cataract Galactose-1-phosphate uridylyltransferase deficiency Inborn errors of carbohydrate metabolism Health Medicine
36	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
37	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
38	INBORN METABOLIC DISORDERS Inborn Metabolic Disorders, called also Inborn Errors of Metabolism, are a large group of genetic diseases caused by malfunctioning of a specific metabolic pathway. A metabolic pathway is a num Add to Reading List Source URL: www.climb.org.uk Language: English - Date: 2014-03-19 09:08:25 Inborn errors of carbohydrate metabolism Inborn error of metabolism Metabolism Pediatrics Medical genetics Galactose-1-phosphate uridylyltransferase deficiency Health Medicine Rare diseases
39	Visio-Hypergalactosemia_4[removed]updated 1009.vsd Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Medicine Galactokinase deficiency Galactose—1-phosphate uridylyltransferase Biology Galactose epimerase deficiency Galactose Galactokinase Galactose-1-phosphate uridylyltransferase deficiency Galactolysis Inborn errors of carbohydrate metabolism Health Galactosemia
40	NUTRITION ISSUES IN GASTROENTEROLOGY, SERIES #41 Carol Rees Parrish, R.D., M.S., Series Editor Add to Reading List Source URL: www.medicine.virginia.edu Language: English - Date: 2011-06-13 10:42:42 Rare diseases Newborn screening Guthrie test Galactose-1-phosphate uridylyltransferase deficiency Medical genetics Galactosemia Biotinidase deficiency Phenylketonuria 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Genetic genealogy

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