Fatty acid metabolism diseases

Evidence-based neurology checklist on fatty acid metabolism diseases: Acyl-CoA dehydrogenase deficiency Short chain (SCAD) Medium chain (MCAD) Long chain (LCAD) Other fatty acid metabolism diseases

Acyl-CoA dehydrogenase deficiency

  • Short chain (SCAD)
  • Medium chain (MCAD)
  • Long chain (LCAD)

Other fatty acid metabolism diseases

References

  1. Sedel F. Inborn errors of metabolism in adult neurology. Rev Neurol (Paris) 2013; 169(Suppl 1):S63-S69.
  2. Gray RGF, Preece MA, Green SH, Whitehouse W, Winer J, Green A. Inborn errors of metabolism as a cause of neurological disease in adults: an approach to investigation. JNNP 2000; 69:5-12.
  3. Christopher R, Sankaran BP. An insight into the biochemistry of inborn errors of metabolism for a clinical neurologist. Ann Indian Acad Neurol 2008; 11:68-81.
  4. Martins AM. Inborn errors of metabolism: a clinical overview. Sao Paulo Med J 1999; 117:251-265.

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