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Description
The underlying cause of very-long-chain acyl-CoA dehydrogenase (VLCAD) deficiency are mutations in the ACADVL gene [101]
It is postulated that clinical symptoms, including CNS complications such as convulsion, coma and lethargy, may be triggered by the accumulation of metabolites and their acyl-CoA derivatives that disrupt intermediary metabolism [6669]
The Behavior of Muscle Oxygen Saturation, Oxy and DeoxyHemoglobin during a Fatigue Test in Fibromyalgia
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The story of Rett syndrome: From clinic to neurobiology
