Galactose-1-phosphate uridyltransferase deficiency (Q40044): Difference between revisions
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| description / pt-br | description / pt-br | ||
Galactosemia clássica é uma doença metabólica grave com início de manifestações no período neonatal. As crianças usualmente desenvolvem dificuldades alimentares, letargia e doença hepática grave. | |||
| description / en | description / en | ||
Classic galactosemia is a life-threatening metabolic disease with onset in the neonatal period. Infants usually develop feeding difficulties, lethargy, and severe liver disease. | |||
Revision as of 05:41, 13 August 2026
Classic galactosemia is a life-threatening metabolic disease with onset in the neonatal period. Infants usually develop feeding difficulties, lethargy, and severe liver disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C51.40 |
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| English | Galactose-1-phosphate uridyltransferase deficiency |
Classic galactosemia is a life-threatening metabolic disease with onset in the neonatal period. Infants usually develop feeding difficulties, lethargy, and severe liver disease. |
