[Glutaric acidemia/glutaric aciduria I as differential chorea minor diagnosis]
- PMID: 8487480
- DOI: 10.1055/s-2007-1025211
[Glutaric acidemia/glutaric aciduria I as differential chorea minor diagnosis]
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.
Similar articles
-
Acute profound dystonia in infants with glutaric acidemia.Pediatrics. 1989 Feb;83(2):228-34. Pediatrics. 1989. PMID: 2643800 Review.
-
Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency.Neuropediatrics. 1996 Jun;27(3):115-23. doi: 10.1055/s-2007-973761. Neuropediatrics. 1996. PMID: 8837070
-
[Glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)].Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):332-5. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9590060 Review. Japanese. No abstract available.
-
Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathy.Pediatrics. 1991 Dec;88(6):1194-203. Pediatrics. 1991. PMID: 1956737
-
Variable clinical and biochemical presentation of seven Spanish cases with glutaryl-CoA-dehydrogenase deficiency.Neuropediatrics. 1995 Oct;26(5):238-42. doi: 10.1055/s-2007-979763. Neuropediatrics. 1995. PMID: 8552212
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical