Fatty acid oxidation disorders definition

Fatty acid oxidation disorders means disorders of metabolism characterized by the inability to efficiently use fat to make energy. When the body needs extra energy, such as during prolonged fasting or acute illness, these disorders can lead to hypoglycemia and metabolic crises resulting in serious damage affecting the brain, liver, heart, eyes, muscle, and possibly death. For the purpose of this chapter fatty acid oxidation disorders include: Carnitine uptake defect (CUD), long-chain L-3-OH acyl-CoA dehydrogenase deficiency (LCHADD), medium-chain acyl-CoA dehydrogenase defi- ciency (MCADD), trifunctional protein deficiency (TFP), and very long-chain acyl-CoA dehydrogenase deficiency (VLCADD).
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Fatty acid oxidation disorders means disorders of metabo­ lism characterized by the inability to efficiently use fat to make en­ ergy. When the body needs extra energy, such as during prolonged fast­ ing or acute illness, these disorders can lead to hypoglycemia and metabolic crises resulting in serious damage affecting the brain, liv­ er, heart, eyes, muscle, and possibly death. For the purpose of this chapter fatty acid oxidation disorders include: Carnitine uptake de­ fect (CUD), long-chain L-3-OH acyl-CoA dehydrogenase deficiency (LCHADD), medium-chain acyl-CoA dehydrogenase deficiency (MCADD), tri­ functional protein deficiency (TFP), and very long-chain acyl-CoA de­ hydrogenase deficiency (VLCADD).
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Fatty acid oxidation disorders means carnitine uptake de- fect (CUD), long-chain L-3-OH acyl-CoA dehydrogenase deficiency (LCHADD), medium-chain acyl-CoA dehydrogenase deficiency (MCADD), tri- functional protein deficiency (TFP), and very long-chain acyl-CoA de- hydrogenase deficiency (VLCADD). These disorders can lead to hypogly- cemia and metabolic crises resulting in serious damage affecting the brain, liver, heart, eyes, muscle, and possibly death.
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Examples of Fatty acid oxidation disorders in a sentence

  • Matern, M.J. Bennett Fatty acid oxidation disorders Annual review of physiology, 64 (2002), 477-502, DOI: 10.1146/annurev.physiol.64.082201.154705.

  • The 28 metabolic disorders currently screened for by the NMSP are:• Amino acid disorders (14 disorders, including PKU and MSUD)• Fatty acid oxidation disorders (9 disorders)• Others:› Congenital hypothyroidism› Cystic fibrosis› Congenital adrenal hyperplasia› Galactosaemia› Biotinidase deficiency.

  • Fatty acid oxidation disorders: outcome and long- term prognosis.

  • Fatty acid oxidation disorders are all inherited as autosomal recessive traits.

  • Fatty acid oxidation disorders are inherited autosomal recessive disorders (Page 5).

  • Fatty acid oxidation disorders, urea cycle defects, types of organo-aciduria, ketolysis defects etc.


More Definitions of Fatty acid oxidation disorders

Fatty acid oxidation disorders means carnitine uptake defect (CUD), long-chain L-3-OH acyl-CoA dehydro- genase deficiency (LCHADD), medium-chain acyl-CoA dehydrogenase deficiency (MCADD), trifunctional protein deficiency (TFP), and very long-chain acyl-CoA dehydroge- nase deficiency (VLCADD). These disorders can lead to hypoglycemia and metabolic crises resulting in serious dam- age affecting the brain, liver, heart, eyes, muscle, and possi- bly death.
Sample 1
Fatty acid oxidation disorders means disor- ders of metabolism characterized by the inability to effi- ciently use fat to make energy. When the body needs extra
Sample 1
Fatty acid oxidation disorders means ((dis- orders of metabolism characterized by the inability to effi- ciently use fat to make energy. When the body needs extra energy, such as during prolonged fasting or acute illness, these disorders can lead to hypoglycemia and metabolic cri- ses resulting in serious damage affecting the brain, liver, heart, eyes, muscle, and possibly death. For the purpose of this chapter fatty acid oxidation disorders include:)) carnitine uptake defect (CUD), long-chain L-3-OH acyl-CoA dehydro- genase deficiency (LCHADD), medium-chain acyl-CoA dehydrogenase deficiency (MCADD), trifunctional protein deficiency (TFP), and very long-chain acyl-CoA dehydroge- nase deficiency (VLCADD). These disorders can lead to hypoglycemia and metabolic crises resulting in serious dam- age affecting the brain, liver, heart, eyes, muscle, and possi- bly death.
Sample 1

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