Rhabdomyolysis in early‐onset very long‐chain acyl‐CoA dehydrogenase deficiency despite normal glucose after fasting

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Abstract
Summary: A patient with very long‐chain acyl‐CoA dehydrogenase (VLCAD) deficiency presented in the neonatal period with hypoketotic hypoglycaemia and at the age of 1 year with rhabdomyolysis and normal glucose after fasting. Rhabdomyolysis may occur in the absence of hypoglycaemia in young infants as well as in older patients.