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

作者信息

Voll R, Hoffmann G F, Lipinski C G, Trefz F K, Weisser J

机构信息

Abteilung: Pädiatrie/Neuropädiatrie, Rehabilitationsklinik Neckargemünd.

出版信息

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

DOI:10.1055/s-2007-1025211
PMID:8487480
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.

摘要

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