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[Hyperuricemia as the main symptom of medium-chain acyl-Co-A dehydrogenase deficiency].

作者信息

Reinehr T, Bürk G, Dietz B, Schlüter B, Andler W

机构信息

Vestische Kinderklinik Datteln, Universität Witten/Herdecke.

出版信息

Klin Padiatr. 1997 Nov-Dec;209(6):357-60. doi: 10.1055/s-2008-1043975.

Abstract

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.

摘要

相似文献

1
[Hyperuricemia as the main symptom of medium-chain acyl-Co-A dehydrogenase deficiency].
Klin Padiatr. 1997 Nov-Dec;209(6):357-60. doi: 10.1055/s-2008-1043975.
2
Fasting medium chain acyl-coenzyme A dehydrogenase--deficient children can make ketones.
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