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Case Reports
. 1993 Mar-Apr;205(2):124-6.
doi: 10.1055/s-2007-1025211.

[Glutaric acidemia/glutaric aciduria I as differential chorea minor diagnosis]

[Article in German]
Affiliations
Case Reports

[Glutaric acidemia/glutaric aciduria I as differential chorea minor diagnosis]

[Article in German]
R Voll et al. Klin Padiatr. 1993 Mar-Apr.

Abstract

Glutaracidemia/glutaraciduria type I is an acute or subacute neuropathic disorder of infancy or early childhood. The following symptoms characterize the clinical course: macrocephalus present at birth, cerebral atrophy revealed by CT or MRI scans, most striking in the frontal and temporal lobes, choreoathetosis and dystonia as neurological handicaps. The deficiency of glutaryl-CoA-dehydrogenase leads to glutaracidemia and glutaraciduria. It is reported on a three year old girl. The glutaraciduria is an important differential diagnosis to chorea minor.

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