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Results 1 - 9 of 9 for Levocarnitine
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  1. Carnitine palmitoyltransferase I deficiency 
    Carnitine palmitoyltransferase I (CPT I) deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods without ...
    https://medlineplus.gov/...rnitine-palmitoyltransferase-i-deficiency - Genetics
  2. 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
  3. Carnitine palmitoyltransferase II deficiency 
    Carnitine palmitoyltransferase II (CPT II) deficiency is a condition that prevents the body from using certain fats ... gene provides instructions for making an enzyme called carnitine palmitoyltransferase 2. This enzyme is essential for fatty ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-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. 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
  6. Isobutyryl-CoA dehydrogenase deficiency 
    ... cells (anemia) and very low blood levels of carnitine, which is a natural substance that helps convert ... disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening. Pediatr ...
    https://medlineplus.gov/.../isobutyryl-coa-dehydrogenase-deficiency - Genetics
  7. Glutaric acidemia type I 
    ... I patients and the protective effects of l-carnitine treatment. J Cell Biochem. 2018 Dec;119(12): ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-i - Genetics
  8. Short/branched chain acyl-CoA dehydrogenase deficiency 
    ... with this condition, a compound called 2-methylbutyryl carnitine is elevated in the blood and another called ...
    https://medlineplus.gov/...d-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  9. Cyclic vomiting syndrome 
    ... vomiting syndrome with combined co-enzyme Q10, L-carnitine and amitriptyline, a case series. BMC Neurol. 2011 ...
    https://medlineplus.gov/genetics/condition/cyclic-vomiting-syndrome - Genetics