| Literature DB >> 6775244 |
R L Leibel, V E Shih, S I Goodman, M L Bauman, E R McCabe, R G Zwerdling, I Bergman, C Costello.
Abstract
A boy with glutaric acidemia had psychomotor retardation first noted at age 6 months, recurrent metabolic acidosis, and a progressive quadriparesis with choreoathetosis. He died at age 3 1/2 years. Cultured skin fibroblasts lacked glutaryl-CoA dehydrogenase activity. There was a biochemical, but not a clinical, response to dietary restriction of lysine and tryptophan. The caudate and putamen of the brain showed severe loss of nerve cells and fibers with proliferation of astrocytes, as well as markedly reduced gamma-aminobutyric acid and glutamate decarboxylase activity.Entities:
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Year: 1980 PMID: 6775244 DOI: 10.1212/wnl.30.11.1163
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910