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Galactose-1-phosphate uridylyltransferase deficiency
Results: 41

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21	Galactosemia Carmen Lozzio, MD University of Tennessee Developmental and Genetics Center Knoxville, Tennessee Outcome without screening: Add to Reading List Source URL: health.tn.gov 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
22	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.tn.gov 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
23	College of Medicine Department of Pediatrics Division of Genetics and Metabolism 1600 SW Archer Road PO Box[removed] Add to Reading List Source URL: www.peds.ufl.edu Language: English - Date: 2013-05-15 11:56:41 Food and drink Galactose-1-phosphate uridylyltransferase deficiency Medicine Galactose Infant formula Breastfeeding Milk Galactose—1-phosphate uridylyltransferase Galactosemic cataract Inborn errors of carbohydrate metabolism Health Galactosemia
24	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: www.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
25	GALACTOSEMIA (Guh-LAK-toe-SEE-me-ah) What is it? Galactosemia is an inherited defect of galactose metabolism caused by an enzyme deficiency in the liver that prevents proper metabolism and utilization of galactose or mil Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-13 16:10:52 Biology Galactosemia Galactose-1-phosphate uridylyltransferase deficiency Galactosemic cataract Inborn errors of carbohydrate metabolism Medicine Health
26	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: www.chfs.ky.gov Language: English - Date: 2014-09-12 08:53:32 Galactose Medicine Milk Galactose-1-phosphate uridylyltransferase deficiency Biology Galactosemic cataract Inborn errors of carbohydrate metabolism Galactosemia Health
27	Newborn Screening for Biotinidase Deficiency Add to Reading List Source URL: www.kdheks.gov Language: English - Date: 2012-02-06 15:23:17 Medicine Food and drink Galactose-1-phosphate uridylyltransferase deficiency Galactosemic cataract Inborn errors of carbohydrate metabolism Health Galactosemia
28	Disease Name Galactosemia Acronym Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 03:19:07 Galactosemia Galactosemic cataract Galactose-1-phosphate uridylyltransferase deficiency Inborn errors of carbohydrate metabolism Health Medicine
29	PDF Document Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2008-08-01 09:35:32 Newborn screening Galactosemia Congenital hypothyroidism Galactose-1-phosphate uridylyltransferase deficiency Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Hypoglycemia Medical genetics Thyroid Genetic testing Medicine Health Pediatrics
30	Newborn Screening Articles Spring[removed]_Clin_Chim_Acta._ 2012 Jul 11;[removed]):[removed]Epub 2012 Mar 23. Amino acid disorders detected by quantitative amino acid HPLC analysis in Thailand: An eight-year experience. _Va Add to Reading List Source URL: genes-r-us.uthscsa.edu Language: English - Date: 2012-07-24 10:19:31 Newborn screening Phenylketonuria Galactosemia Neonatal jaundice Galactose-1-phosphate uridylyltransferase deficiency Screening Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Neonatology Cystic fibrosis Medicine Health Pediatrics

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