Reinehr T, Bürk G, Dietz B, Schlüter B, Andler W
Vestische Kinderklinik Datteln, Universität Witten/Herdecke.
Klin Padiatr. 1997 Nov-Dec;209(6):357-60. doi: 10.1055/s-2008-1043975.
Between 1991 and 1996 three cases of MCAD-deficiency (medium-chain-acyl-Co-A dehydrogenase deficiency) were diagnosed in the Vestische Kinderklinik. All patients showed hypoketotic hypoglycaemia with hyperuricaemia. In the group of hypoketotic hypoglycaemia without lactat acidosis MCAD-deficiency is the only metabolic disease presenting regularly with hyperuricaemia. Thus, hyperuricaemia in a patient with hypoketotic hypoglycaemia is a strong indicator for MCAD-deficiency. Measurement of uric acid is easily available before sophisticated metabolic analysis are completed.