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Results 1 - 10 of 25 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. slc25a20 
    ... 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
  3. carnitine-acylcarnitine-translocase-deficiency 
    Carnitine-acylcarnitine translocase (CACT) deficiency is a condition that prevents the body from using certain fats for ...
    https://medlineplus.gov/...tine-acylcarnitine-translocase-deficiency - Genetics
  4. cpt1a 
    ... 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
  5. carnitine-palmitoyltransferase-i-deficiency 
    Carnitine palmitoyltransferase I (CPT I) deficiency is a condition that prevents the body from using certain fats for energy. The signs and symptoms of CPT I deficiency ...
    https://medlineplus.gov/...rnitine-palmitoyltransferase-i-deficiency - Genetics
  6. slc22a5 
    ... 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
  7. carnitine-palmitoyltransferase-ii-deficiency 
    Carnitine palmitoyltransferase II (CPT II) deficiency is a condition that prevents the body from using certain fats ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-deficiency - Genetics
  8. cpt2 
    ... 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
  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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