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Date: 2014-04-04 11:40:11Galactosemia Galactose epimerase deficiency Galactokinase deficiency Newborn screening Galactosemic cataract Galactokinase UDP-glucose 4-epimerase Cataract Genetic disorder Inborn errors of carbohydrate metabolism Health Medicine | 2012 Minnesota Department of Health (ga-lac-toe-see-me-ah) POSITIVE NEWBORN SCREENAdd to Reading ListSource URL: www.health.state.mn.usDownload Document from Source WebsiteFile Size: 176,96 KBShare Document on Facebook |
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Galactosemia Testing Algorithm ■ ■ ■ Clinical suspicion of classic galactosemiaDocID: RHr3 - View Document | |
May[removed]Volume 30 Number 5 FeatureDocID: Rzle - View Document | |
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 causeDocID: KflU - View Document | |
Galactosemia Carmen Lozzio, MD University of Tennessee Developmental and Genetics Center Knoxville, Tennessee Outcome without screening:DocID: HxhA - View Document |