Alpha-ketoglutarate dehydrogenase deficiency (Q93769): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Verification Status | |||
Concluído | |||
| Property / Verification Status: Concluído / rank | |||
Normal rank | |||
Revision as of 08:52, 16 August 2026
Oxoglutaric aciduria is a tricarboxylic acid cycle disorder caused by deficiency of alpha ketoglutarate dehydrogenase (oxoglutarate dehydrogenase), characterised by severe psychomotor retardation, hypotonia, ataxia and convulsions (the signs of Leigh's syndrome), as well as sudden death, myocardiopathy, and hepatic disorders.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1273268933 |
||
| English | Alpha-ketoglutarate dehydrogenase deficiency |
Oxoglutaric aciduria is a tricarboxylic acid cycle disorder caused by deficiency of alpha ketoglutarate dehydrogenase (oxoglutarate dehydrogenase), characterised by severe psychomotor retardation, hypotonia, ataxia and convulsions (the signs of Leigh's syndrome), as well as sudden death, myocardiopathy, and hepatic disorders. |
Statements
CID11:ID_1273268933
0 references
dki-india-ID_1273268933
0 references
Concluído
0 references
