May[removed]Volume 30 Number 5 Feature

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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		May[removed]Volume 30 Number 5 Feature Add to Reading List Source URL: www.mayomedicallaboratories.com Download Document from Source Website File Size: 405,26 KB Share Document on Facebook

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	Galactosemia Testing Algorithm ■ ■ ■ Clinical suspicion of classic galactosemia DocID: RHr3 - View Document
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	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 DocID: KflU - View Document
	Galactosemia Carmen Lozzio, MD University of Tennessee Developmental and Genetics Center Knoxville, Tennessee Outcome without screening: DocID: HxhA - View Document