Inborn errors of glycosylation or other specified protein modification (Q40196): Difference between revisions
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Os distúrbios congênitos de glicosilação (CDG) são um grupo de distúrbios de síntese de glicoproteína caracterizados por manifestações neurológicas que podem ser associadas ao envolvimento multivisceral. As síndromes do CDG estão associadas a diferentes déficits enzimáticos. | |||
| description / en | description / en | ||
Congenital Disorders of Glycosylation (CDG) syndromes are a group of glycoprotein synthesis disorders characterised by neurological manifestations that can be associated with multivisceral involvement. The CDG syndromes are associated with different enzymatic deficits. | |||
Revision as of 05:55, 13 August 2026
Congenital Disorders of Glycosylation (CDG) syndromes are a group of glycoprotein synthesis disorders characterised by neurological manifestations that can be associated with multivisceral involvement. The CDG syndromes are associated with different enzymatic deficits.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C54 |
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| English | Inborn errors of glycosylation or other specified protein modification |
Congenital Disorders of Glycosylation (CDG) syndromes are a group of glycoprotein synthesis disorders characterised by neurological manifestations that can be associated with multivisceral involvement. The CDG syndromes are associated with different enzymatic deficits. |
