Carnitine palmitoyltransferase II deficiency, neonatal form (Q104472): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A forma neonatal da deficiência de carnitina palmitoiltransferase II, um distúrbio hereditário que afeta a oxidação mitocondrial de ácidos graxos de cadeia longa, é a forma letal da doença que se apresenta com insuficiência de multiplos órgãos. | |||
| description / en | description / en | ||
The neonatal form of carnitine palmitoyltransferase II (CPT II) deficiency, an inherited disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the lethal form of the disease which presents with multisystem failure. | |||
Revision as of 10:19, 17 August 2026
The neonatal form of carnitine palmitoyltransferase II (CPT II) deficiency, an inherited disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the lethal form of the disease which presents with multisystem failure.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1280842213 |
||
| English | Carnitine palmitoyltransferase II deficiency, neonatal form |
The neonatal form of carnitine palmitoyltransferase II (CPT II) deficiency, an inherited disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the lethal form of the disease which presents with multisystem failure. |
