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. 2018 Oct 10;19(1):43–48. doi: 10.1136/practneurol-2018-002008

Table 2.

Summary of inherited metabolic causes of exertional rhabdomyolysis

Metabolic pathway Trigger Baseline CK Baseline weakness Examples
Glycogen metabolism Early onset after intense exercise Often high May develop in later life
  • McArdle’s disease (second wind phenomenon)

  • Tarui’s syndrome (↑exercise tolerance when fasting, compensated haemolysis)

  • Lactate dehydrogenase-A deficiency (photosensitive rash)

Fatty acid metabolism Later onset after prolonged exercise or illness/fasting Normal Unusual
  • Carnitine palmitoyltransferase (diffuse exertional weakness, respiratory failure)

Mitochondrial metabolism Early or late onset, prominent fatigue Normal or high Possible
  • Coenzyme Q10 (encephalopathy, ataxia, convulsions)

  • Cytochrome B/C (onset after mild exercise)

CK, creatine kinase.