Glutaric aciduria type 1 (Q64120): Difference between revisions
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Revision as of 11:39, 14 August 2026
Glutaric acidemia type 1 is an inborn error of lysine and triptophan metabolism due to glutaryl-Coenzyme A (CoA) dehydrogenase deficiency clinically characterised by a acute encephalopathy that results in bilateral striatal damage leading to a severe dystonic dyskinetic movement disorder.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1749323401 |
||
| English | Glutaric aciduria type 1 |
Glutaric acidemia type 1 is an inborn error of lysine and triptophan metabolism due to glutaryl-Coenzyme A (CoA) dehydrogenase deficiency clinically characterised by a acute encephalopathy that results in bilateral striatal damage leading to a severe dystonic dyskinetic movement disorder. |
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CID11:ID_1749323401
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dki-india-ID_1749323401
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Concluído
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