Galactokinase deficiency (Q40041): Difference between revisions
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Deficiência de galactoquinase é uma forma leve de galactosemia caracterizada por início precoce de catarata e ausência dos sinais usuais de galactosemia clássica, ou seja, dificuldade de alimentação, comprometimento do crescimento e ganho de peso, letargia e icterícia. | |||
| description / en | description / en | ||
Galactokinase deficiency is a rare mild form of galactosemia characterised by early onset of cataract and an absence of the usual signs of classic galactosemia, i.e. feeding difficulties, poor weight gain and growth, lethargy, and jaundice. | |||
Revision as of 05:41, 13 August 2026
Galactokinase deficiency is a rare mild form of galactosemia characterised by early onset of cataract and an absence of the usual signs of classic galactosemia, i.e. feeding difficulties, poor weight gain and growth, lethargy, and jaundice.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C51.41 |
||
| English | Galactokinase deficiency |
Galactokinase deficiency is a rare mild form of galactosemia characterised by early onset of cataract and an absence of the usual signs of classic galactosemia, i.e. feeding difficulties, poor weight gain and growth, lethargy, and jaundice. |
