Carnitine transporter deficiency (Q91986): Difference between revisions
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15 August 2026
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Latest revision as of 07:08, 16 August 2026
Carnitine uptake deficiency is a fatty acid disorder due to defective carnitine transporters, resulting in progressive hypokinetic dilated cardiomyopathy that is generally associated with muscular weakness. This last sign may be major and result in proximal myopathy and amyotrophy. Hypoglycaemia- and hypoketosis-linked coma or acute hepatic injuries such as Reye's syndrome may occur after periods of fasting or infections.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_526376450 |
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| English | Carnitine transporter deficiency |
Carnitine uptake deficiency is a fatty acid disorder due to defective carnitine transporters, resulting in progressive hypokinetic dilated cardiomyopathy that is generally associated with muscular weakness. This last sign may be major and result in proximal myopathy and amyotrophy. Hypoglycaemia- and hypoketosis-linked coma or acute hepatic injuries such as Reye's syndrome may occur after periods of fasting or infections. |
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CID11:ID_526376450
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dki-india-ID_526376450
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Concluído
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15 August 2026
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