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Results 1 - 10 of 20 for Oxidation
  1. 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... dehydrogenase.Normally, through a process called fatty acid oxidation, several enzymes work in a step-wise fashion ... CoA dehydrogenase deficiency, are known as fatty acid oxidation disorders. HADH This condition is inherited in an ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  2. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... JP, Attie-Bitach T. Long-chain fatty acid oxidation during early human development. Pediatr Res. 2005 Jun; ... Rinaldo P, Matern D, Bennett MJ. Fatty acid oxidation disorders. Annu Rev Physiol. 2002;64:477-502. ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  3. Mitochondrial trifunctional protein deficiency 
    ... Mitochondrial trifunctional protein deficiency: a severe fatty acid oxidation disorder with cardiac and neurologic involvement. J Pediatr. ... JP, Attie-Bitach T. Long-chain fatty acid oxidation during early human development. Pediatr Res. 2005 Jun; ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
  4. Very long-chain acyl-CoA dehydrogenase deficiency 
    ... Asselbergs FW, Houtkooper RH, Visser G. Fatty acid oxidation flux predicts the clinical severity of VLCAD deficiency. ...
    https://medlineplus.gov/...g-chain-acyl-coa-dehydrogenase-deficiency - Genetics
  5. ACAD9 deficiency 
    ... enzyme also plays a role in fatty acid oxidation, a multistep process that occurs within mitochondria to ... assembly as well as long-chain fatty acid oxidation, while others affect only complex I assembly. The ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  6. Carnitine palmitoyltransferase I deficiency 
    ... Carnitine palmitoyltransferase 1A is essential for fatty acid oxidation, which is the multistep process that breaks down ( ... fats and converts them into energy. Fatty acid oxidation takes place within mitochondria, which are the energy- ...
    https://medlineplus.gov/...rnitine-palmitoyltransferase-i-deficiency - Genetics
  7. Chanarin-Dorfman syndrome 
    ... storage disease with impaired long-chain fatty acid oxidation Genetic Testing Registry: Triglyceride storage disease with ichthyosis ...
    https://medlineplus.gov/genetics/condition/chanarin-dorfman-syndrome - Genetics
  8. Familial lipoprotein lipase deficiency 
    Familial lipoprotein lipase deficiency is an inherited condition that disrupts the normal breakdown of fats in the body, resulting in an increase of certain kinds ...
    https://medlineplus.gov/.../familial-lipoprotein-lipase-deficiency - Genetics
  9. 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
  10. Glutaric acidemia type II 
    Glutaric acidemia type II is an inherited disorder that interferes with the body's ability to break down proteins and fats to produce energy. Incompletely processed ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-ii - Genetics
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