Literature DB >> 7247788

Pyruvate decarboxylase deficiency in subacute necrotizing encephalomyelopathy.

O B Evans.   

Abstract

A partial deficiency of pyruvate decarboxylase (PDC) was demonstrated in a child with hyperlactatemia and progressive ataxia, bulbar paresis, ophthalmoplegia, and polyneuropathy. Subacute necrotizing encephalomyelopathy (SNE) was found at necropsy. The association of SNE and PDC deficiency has been reported rarely, but a review of the diverse metabolic defects associated with SNE suggests that decreased PDC activity may be the common feature of SNE.

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Year:  1981        PMID: 7247788     DOI: 10.1001/archneur.1981.00510080077012

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  10 in total

1.  Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.

Authors:  S Miyabayashi; T Ito; K Narisawa; K Iinuma; K Tada
Journal:  Eur J Pediatr       Date:  1985-03       Impact factor: 3.183

Review 2.  Disorders of the pyruvate dehydrogenase complex.

Authors:  D Stansbie; S J Wallace; C Marsac
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

Review 3.  Mitochondrial myopathies. Clinical, morphological and biochemical aspects.

Authors:  R C Sengers; A M Stadhouders; J M Trijbels
Journal:  Eur J Pediatr       Date:  1984-02       Impact factor: 3.183

4.  [Diagnostic significance of muscle biopsies in metabolic myopathies. II. Clinical biochemistry].

Authors:  T Deufel; I Paetzke; D Pongratz; G Hübner; O H Wieland
Journal:  Klin Wochenschr       Date:  1984-07-16

5.  A case of pyruvate carboxylase deficiency with later prenatal diagnosis of an unaffected sibling.

Authors:  A Tsuchiyama; K Oyanagi; S Hirano; N Tachi; H Sogawa; K Wagatsuma; T Nakao; S Tsugawa; Y Kawamura
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

6.  Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.

Authors:  P M van Erven; F J Gabreëls; W Ruitenbeek; W O Renier; K J Lamers; J L Sloof
Journal:  J Neurol       Date:  1987-05       Impact factor: 4.849

7.  Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE).

Authors:  B Kustermann-Kuhn; K Harzer; R Schröder; W Permanetter; J Peiffer
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Fatal lactic acidosis due to deficiency of E1 component of the pyruvate dehydrogenase complex.

Authors:  M A Birch-Machin; I M Shepherd; M Solomon; S J Yeaman; D Gardner-Medwin; H S Sherratt; J G Lindsay; A Aynsley-Green; D M Turnbull
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

9.  Familial dystonia and visual failure with striatal CT lucencies.

Authors:  C D Marsden; A E Lang; N P Quinn; W I McDonald; A Abdallat; S Nimri
Journal:  J Neurol Neurosurg Psychiatry       Date:  1986-05       Impact factor: 10.154

10.  X-linked Leigh's syndrome.

Authors:  P J Benke; J C Parker; M L Lubs; J Benkendorf; A E Feuer
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

  10 in total

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