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Results 1 - 10 of 40 for Levocarnitine
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  1. Primary carnitine deficiency 
    Primary carnitine deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods without food (fasting). Carnitine, ...
    https://medlineplus.gov/.../condition/primary-carnitine-deficiency - Genetics
  2. Carnitine palmitoyltransferase II deficiency 
    Carnitine palmitoyltransferase II (CPT II) deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods of fasting. ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-deficiency - Genetics
  3. Carnitine palmitoyltransferase I deficiency 
    Carnitine palmitoyltransferase I (CPT I) deficiency is a condition that prevents the body from using certain fats ... deficiency have high levels of a compound called carnitine. Cells use carnitine, a natural substance that is ...
    https://medlineplus.gov/...rnitine-palmitoyltransferase-i-deficiency - Genetics
  4. Carnitine-acylcarnitine translocase deficiency 
    Carnitine-acylcarnitine translocase (CACT) deficiency is a condition that prevents the body from using certain fats for ... gene provides instructions for making a protein called carnitine-acylcarnitine translocase (CACT). This protein is essential for ...
    https://medlineplus.gov/...tine-acylcarnitine-translocase-deficiency - Genetics
  5. SLC22A5 gene 
    ... membrane, where it transports a substance known as carnitine into the cell. Carnitine is mainly obtained from food and is needed ... SLC22A5 gene have been found to cause primary carnitine deficiency. Some of these variants create a premature ...
    https://medlineplus.gov/genetics/gene/slc22a5 - Genetics
  6. CPT1A gene 
    ... gene provides instructions for making an enzyme called carnitine palmitoyltransferase 1A, which is found in the liver. ... first be attached to a substance known as carnitine. Carnitine palmitoyltransferase 1A connects carnitine to long-chain ...
    https://medlineplus.gov/genetics/gene/cpt1a - Genetics
  7. CPT2 gene 
    ... gene provides instructions for making an enzyme called carnitine palmitoyltransferase 2. This enzyme is essential for fatty ... acids must first attach to a compound called carnitine. Once inside mitochondria, carnitine palmitoyltransferase 2 removes the ...
    https://medlineplus.gov/genetics/gene/cpt2 - Genetics
  8. SLC25A20 gene 
    ... gene provides instructions for making a protein called carnitine-acylcarnitine translocase (CACT). This protein is essential for ... must be attached to a substance known as carnitine to enter mitochondria. Once these fatty acids are ...
    https://medlineplus.gov/genetics/gene/slc25a20 - Genetics
  9. Short-chain acyl-CoA dehydrogenase deficiency 
    ... disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening. Pediatr ...
    https://medlineplus.gov/...t-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  10. Lipid Metabolism Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
    https://medlineplus.gov/lipidmetabolismdisorders.html - Health Topics
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