Pyruvate dehydrogenase deficiency restricted to brain
- PMID: 6783978
- DOI: 10.1212/wnl.31.4.398
Pyruvate dehydrogenase deficiency restricted to brain
Abstract
We studied a child with a rapidly progressive neurologic disorder, with psychomotor retardation, hypotonia, seizures, and respiratory disturbances. Laboratory studied showed elevated levels of lactate and pyruvate in cerebrospinal fluid (CSF), without notable elevated levels in serum. In liver, muscle, leukocytes, and cultured fibroblasts we found no abnormality in pyruvate oxidation; biochemical studies of a brain biopsy showed an isolated deficiency of pyruvate dehydrogenase complex in brain tissue with the morphologic picture of progressive poliodystrophy with hypomyelination.
Similar articles
-
Progressive infantile poliodystrophy (Alpers' disease) with a defect in citric acid cycle activity in liver and fibroblasts.Neuropediatrics. 1982 May;13(2):108-11. doi: 10.1055/s-2008-1059608. Neuropediatrics. 1982. PMID: 6813759
-
Defects in citric acid cycle and the electron transport chain in progressive poliodystrophy.Acta Neurol Scand. 1984 Sep;70(3):145-54. doi: 10.1111/j.1600-0404.1984.tb00813.x. Acta Neurol Scand. 1984. PMID: 6439001
-
"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis.Eur J Pediatr. 1988 Jan;147(1):10-4. doi: 10.1007/BF00442603. Eur J Pediatr. 1988. PMID: 3123240
-
[Enzymopathic congenital hyperlactacidemia].Ann Biol Clin (Paris). 1976;34(2):151-9. Ann Biol Clin (Paris). 1976. PMID: 184725 Review. French.
-
Defects of pyruvate metabolism and the Krebs cycle.J Child Neurol. 2002 Dec;17 Suppl 3:3S26-33; discussion 3S33-4. J Child Neurol. 2002. PMID: 12597053 Review.
Cited by
-
Neuropathology in cerebral lactic acidosis.Acta Neuropathol. 1987;74(4):393-6. doi: 10.1007/BF00687218. Acta Neuropathol. 1987. PMID: 3687391
-
Disorders of the pyruvate dehydrogenase complex.J Inherit Metab Dis. 1986;9(2):105-19. doi: 10.1007/BF01799447. J Inherit Metab Dis. 1986. PMID: 3018357 Review.
-
Lipoamidase (lipoyl-X hydrolase) from pig brain.Biochem J. 1990 Mar 1;266(2):427-34. doi: 10.1042/bj2660427. Biochem J. 1990. PMID: 2317196 Free PMC article.
-
The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.Mol Genet Metab. 2012 Jul;106(3):385-94. doi: 10.1016/j.ymgme.2012.03.017. Mol Genet Metab. 2012. PMID: 22896851 Free PMC article.
-
Mutation of E1 alpha gene in a female patient with pyruvate dehydrogenase deficiency due to rapid degradation of E1 protein.J Inherit Metab Dis. 1992;15(6):848-56. doi: 10.1007/BF01800220. J Inherit Metab Dis. 1992. PMID: 1338114
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical