Carnitine palmitoyltransferase I deficiency (Q91979): 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 07:08, 16 August 2026
Carnitine palmitoyltransferase 1A (CPT-1A) deficiency is an inborn error of metabolism that affects mitochondrial oxidation of long chain fatty acids (LCFA) in the liver and kidneys, and is characterised by recurrent attacks of fasting-induced hypoketotic hypoglycaemia and risk of liver failure.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_500237301 |
||
| English | Carnitine palmitoyltransferase I deficiency |
Carnitine palmitoyltransferase 1A (CPT-1A) deficiency is an inborn error of metabolism that affects mitochondrial oxidation of long chain fatty acids (LCFA) in the liver and kidneys, and is characterised by recurrent attacks of fasting-induced hypoketotic hypoglycaemia and risk of liver failure. |
Statements
CID11:ID_500237301
0 references
dki-india-ID_500237301
0 references
Concluído
0 references
15 August 2026
0 references
