Glutaric aciduria type 1 (Q64120): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (2 intermediate revisions by the same user not shown) | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 11:40, 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. |
Statements
CID11:ID_1749323401
0 references
dki-india-ID_1749323401
0 references
Concluído
0 references
13 August 2026
0 references
