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- Duarte_galactosemia abstract "Duarte galactosemia (also known as Duarte variant galactosemia, DG, or biochemical variant galactosemia) is an inherited condition associated with diminished ability to metabolize galactose due to a partial deficiency of the enzyme galactose-1-phosphate uridylyltransferase Duarte galactosemia (DG) is estimated to affect close to one in 4,000 infants born in the United States. DG Is considered by most healthcare professionals to be clinically mild. It differs from classic galactosemia in that patients with Duarte galactosemia have partial GALT deficiency whereas patients with classic galactosemia have complete, or almost complete, GALT deficiency.DG, and the possible outcomes associated with this condition, are currently not well understood. Due to regional variations in newborn screening (NBS) protocols, some infants with DG are identified by NBS but others are not. In addition, of the infants who are diagnosed, most are clinically healthy as babies and toddlers, resulting in early discharge from follow up. Many healthcare professionals believe that DG does not negatively impact development. However, some reports have indicated that children with DG may be at increased risk for some developmental problems.".
- Duarte_galactosemia thumbnail Leloir_pathway_cropped.jpg?width=300.
- Duarte_galactosemia wikiPageExternalLink duartegalactosemia.org.
- Duarte_galactosemia wikiPageExternalLink www.galactosemia.org.
- Duarte_galactosemia wikiPageExternalLink NBK258640.
- Duarte_galactosemia wikiPageExternalLink intervention-and-outcomes-duarte-galactosemia.
- Duarte_galactosemia wikiPageID "48328196".
- Duarte_galactosemia wikiPageLength "18197".
- Duarte_galactosemia wikiPageOutDegree "16".
- Duarte_galactosemia wikiPageRevisionID "701676174".
- Duarte_galactosemia wikiPageWikiLink Category:Galactose.
- Duarte_galactosemia wikiPageWikiLink Category:Metabolic_disorders.
- Duarte_galactosemia wikiPageWikiLink Dominance_(genetics).
- Duarte_galactosemia wikiPageWikiLink Galactokinase_deficiency.
- Duarte_galactosemia wikiPageWikiLink Galactose.
- Duarte_galactosemia wikiPageWikiLink Galactose-1-phosphate_uridylyltransferase.
- Duarte_galactosemia wikiPageWikiLink Galactose-1-phosphate_uridylyltransferase_deficiency.
- Duarte_galactosemia wikiPageWikiLink Galactose_epimerase_deficiency.
- Duarte_galactosemia wikiPageWikiLink Galactosemia.
- Duarte_galactosemia wikiPageWikiLink Glycogen_storage_disease_type_XI.
- Duarte_galactosemia wikiPageWikiLink Leloir_pathway.
- Duarte_galactosemia wikiPageWikiLink Mutation.
- Duarte_galactosemia wikiPageWikiLink Neonatal_jaundice.
- Duarte_galactosemia wikiPageWikiLink Newborn_screening.
- Duarte_galactosemia wikiPageWikiLink File:DG_autosomal_recessive_cropped.jpeg.
- Duarte_galactosemia wikiPageWikiLink File:Leloir_pathway_cropped.jpg.
- Duarte_galactosemia wikiPageWikiLinkText "Duarte galactosemia".
- Duarte_galactosemia wikiPageUsesTemplate Template:Cite_book.
- Duarte_galactosemia wikiPageUsesTemplate Template:Medicine.
- Duarte_galactosemia subject Category:Galactose.
- Duarte_galactosemia subject Category:Metabolic_disorders.
- Duarte_galactosemia hypernym Condition.
- Duarte_galactosemia type Disease.
- Duarte_galactosemia comment "Duarte galactosemia (also known as Duarte variant galactosemia, DG, or biochemical variant galactosemia) is an inherited condition associated with diminished ability to metabolize galactose due to a partial deficiency of the enzyme galactose-1-phosphate uridylyltransferase Duarte galactosemia (DG) is estimated to affect close to one in 4,000 infants born in the United States. DG Is considered by most healthcare professionals to be clinically mild.".
- Duarte_galactosemia label "Duarte galactosemia".
- Duarte_galactosemia wasDerivedFrom Duarte_galactosemia?oldid=701676174.
- Duarte_galactosemia depiction Leloir_pathway_cropped.jpg.
- Duarte_galactosemia isPrimaryTopicOf Duarte_galactosemia.