Multiple acyl-CoA dehydrogenase deficiency (Q93446): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 08:33, 16 August 2026
Multiple FAD dehydrogenase deficiency, also known as glutaric aciduria type II, is a disorder of fatty acid oxidation, of branched aminoacids, lysine and glutaric acid. The enzymatic deficiency can be complete causing severe disorders in neonates, to incomplete (Juvenile, adolescent or even adult forms) that are less severe, with progressive myocardiopathy or proximal myopathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_977130875 |
||
| English | Multiple acyl-CoA dehydrogenase deficiency |
Multiple FAD dehydrogenase deficiency, also known as glutaric aciduria type II, is a disorder of fatty acid oxidation, of branched aminoacids, lysine and glutaric acid. The enzymatic deficiency can be complete causing severe disorders in neonates, to incomplete (Juvenile, adolescent or even adult forms) that are less severe, with progressive myocardiopathy or proximal myopathy. |
Statements
CID11:ID_977130875
0 references
dki-india-ID_977130875
0 references
Concluído
0 references
15 August 2026
0 references
