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Results 1 - 8 of 8 for Carnitine deficiency
  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 I deficiency 
    ... type I CPT I deficiency Liver form of carnitine palmitoyltransferase deficiency Genetic Testing Registry: Carnitine palmitoyl transferase 1A deficiency ...
    https://medlineplus.gov/...rnitine-palmitoyltransferase-i-deficiency - Genetics
  3. Carnitine-acylcarnitine translocase deficiency 
    ... signs and symptoms of the condition. CACT deficiency Carnitine acylcarnitine translocase deficiency Carnitine-acylcarnitine carrier deficiency Genetic Testing Registry: Carnitine ...
    https://medlineplus.gov/...tine-acylcarnitine-translocase-deficiency - Genetics
  4. Carnitine palmitoyltransferase II deficiency 
    ... not show signs and symptoms of the condition. Carnitine palmitoyltransferase 2 deficiency CPT II deficiency CPT2 deficiency Genetic Testing Registry: ...
    https://medlineplus.gov/...nitine-palmitoyltransferase-ii-deficiency - Genetics
  5. Short-chain acyl-CoA dehydrogenase deficiency 
    Short-chain acyl-CoA dehydrogenase (SCAD) deficiency is a condition that prevents the body from converting certain fats into energy, especially during periods ...
    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 certain foods into energy. The range of signs and symptoms associated with IBD deficiency remains unclear because very few affected individuals have ...
    https://medlineplus.gov/.../isobutyryl-coa-dehydrogenase-deficiency - Genetics
  7. Short/branched chain acyl-CoA dehydrogenase deficiency 
    ... with this condition, a compound called 2-methylbutyryl carnitine is elevated in the blood and another called 2-methylbutyrylglycine is elevated in the urine (2-methylbutyrylglycinuria).Most people with SBCAD deficiency have no health problems related to the disorder. ...
    https://medlineplus.gov/...d-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  8. Glutaric acidemia type I 
    ... I patients and the protective effects of l-carnitine treatment. J Cell Biochem. 2018 Dec;119(12): ... in children and adults with glutaryl-CoA dehydrogenase deficiency. Pediatr Res. 2006 Jun;59(6):840-7. ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-i - Genetics