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Current and Future Treatments for Classic Galactosemia
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911353/
- Type I (classic) galactosemia, galactose 1-phosphate uridylyltransferase (GALT)-deficiency is a hereditary disorder of galactose metabolism. The current …
- https://pubmed.ncbi.nlm.nih.gov/27858262/
- International clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up. Classical galactosemia (CG) is an inborn error of galactose …
Galactosemia: Clinical, Genetic, and Biochemical Study
- https://jamanetwork.com/journals/jama/article-abstract/332227
- GALACTOSEMIA is a hereditary disorder of carbohydrate metabolism characterized by vomiting, diarrhea, jaundice, poor weight gain, and malnutrition during …
The natural history of classic galactosemia: lessons from …
- https://ojrd.biomedcentral.com/articles/10.1186/s13023-019-1047-z
- Classic galactosemia is a rare inborn error of carbohydrate metabolism, caused by a severe deficiency of the enzyme galactose-1-phosphate uridylyltransferase …
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