<--- Back to Details
First PageDocument Content
Galactosemia / Galactose epimerase deficiency / Galactokinase deficiency / Newborn screening / Galactosemic cataract / Galactokinase / UDP-glucose 4-epimerase / Cataract / Genetic disorder / Inborn errors of carbohydrate metabolism / Health / Medicine
Date: 2014-04-04 11:40:11
Galactosemia
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 SCREEN

Add to Reading List

Source URL: www.health.state.mn.us

Download Document from Source Website

File Size: 176,96 KB

Share Document on Facebook

Similar Documents

Medical statistics / Medicine / Ophthalmology / Cataract / Incidence / Glaucoma / Prevalence / Cataract surgery / Galactosemic cataract / Blindness / Epidemiology / Health

PDF Document

DocID: 179hp - View Document

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

Galactosemia Testing Algorithm ■ ■ ■ Clinical suspicion of classic galactosemia

DocID: RHr3 - View Document

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

DocID: Rzle - View Document

Galactosemia / Galactose-1-phosphate uridylyltransferase deficiency / Galactosemic cataract / Inborn errors of carbohydrate metabolism / Medicine / Health

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 / Biology / Galactose-1-phosphate uridylyltransferase deficiency / Galactose—1-phosphate uridylyltransferase / Galactosemic cataract / Galactokinase / Galactitol / Galactose / Newborn screening / Inborn errors of carbohydrate metabolism / Health / Medicine

Galactosemia Carmen Lozzio, MD University of Tennessee Developmental and Genetics Center Knoxville, Tennessee Outcome without screening:

DocID: HxhA - View Document