Literature DB >> 3687391

Neuropathology in cerebral lactic acidosis.

C W Chow1, R M Anderson, G C Kenny.   

Abstract

The neuropathology in two young infants with cerebral lactic acidosis is presented. Both cases showed microcephaly, ventricular dilatation, absent corpus callosum, absent or extremely hypoplastic pyramids, heterotopic inferior olives, focal neuroglial overgrowth into meninges, focal cystic change with gliosis and recent degenerative changes in the germinal matrix. The cerebellum, basal ganglia, Ammon's horn, inferior colliculi and layering of the cortex were well preserved. The features suggest a continuous damage with very old, relatively old and recent lesions. This striking combination of abnormalities should raise the possibility of a disturbance of lactate/pyruvate metabolism.

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Year:  1987        PMID: 3687391     DOI: 10.1007/bf00687218

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  13 in total

1.  [Cortical neuronal immaturity with agenesis of the major interhemispherical commissures and hypoplasia of the optico-pyramidal tracts in 3 children of the same family].

Authors:  G C Guazzi; G Stoppoloni; V Ventruto; G Di Iorio
Journal:  Acta Neurol (Napoli)       Date:  1974 Nov-Dec

2.  The activity of pyruvate dehydrogenase in rat brain during postnatal development.

Authors:  J E Cremer; H M Teal
Journal:  FEBS Lett       Date:  1974-02-01       Impact factor: 4.124

3.  Storage of skin biopsies at -70 degrees C for future fibroblast culture.

Authors:  K J Fowler
Journal:  J Clin Pathol       Date:  1984-10       Impact factor: 3.411

4.  Cerebro-ocular dysgenesis (Walker-Warburg syndrome): neuropathologic and etiologic analysis.

Authors:  R S Williams; C N Swisher; M Jennings; M Ambler; V S Caviness
Journal:  Neurology       Date:  1984-12       Impact factor: 9.910

5.  The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detection.

Authors:  A Roscher; B Molzer; H Bernheimer; S Stöckler; I Mutz; F Paltauf
Journal:  Pediatr Res       Date:  1985-09       Impact factor: 3.756

6.  What causes infarction in ischemic brain?: The Robert Wartenberg Lecture.

Authors:  F Plum
Journal:  Neurology       Date:  1983-02       Impact factor: 9.910

7.  Pyruvate dehydrogenase deficiency restricted to brain.

Authors:  M Prick; F Gabreëls; W Renier; F Trijbels; H Jaspar; K Lamers; J Kok
Journal:  Neurology       Date:  1981-04       Impact factor: 9.910

8.  beta-hydroxyisobutyryl coenzyme A deacylase deficiency: a defect in valine metabolism associated with physical malformations.

Authors:  G K Brown; S M Hunt; R Scholem; K Fowler; A Grimes; J F Mercer; R M Truscott; R G Cotton; J G Rogers; D M Danks
Journal:  Pediatrics       Date:  1982-10       Impact factor: 7.124

9.  "Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis.

Authors:  G K Brown; E A Haan; D M Kirby; R D Scholem; J E Wraith; J G Rogers; D M Danks
Journal:  Eur J Pediatr       Date:  1988-01       Impact factor: 3.183

10.  The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosis.

Authors:  B H Robinson; J Taylor; W G Sherwood
Journal:  Pediatr Res       Date:  1980-08       Impact factor: 3.756

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  18 in total

Review 1.  The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.

Authors:  Kavi P Patel; Thomas W O'Brien; Sankarasubramon H Subramony; Jonathan Shuster; Peter W Stacpoole
Journal:  Mol Genet Metab       Date:  2011-10-07       Impact factor: 4.797

2.  The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.

Authors:  Kavi P Patel; Thomas W O'Brien; Sankarasubramon H Subramony; Jonathan Shuster; Peter W Stacpoole
Journal:  Mol Genet Metab       Date:  2012-07       Impact factor: 4.797

Review 3.  Magnetic resonance imaging in lactic acidosis.

Authors:  M S van der Knaap; C Jakobs; J Valk
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

Review 4.  Neuropathology and pathogenesis of mitochondrial diseases.

Authors:  G K Brown; M V Squier
Journal:  J Inherit Metab Dis       Date:  1996       Impact factor: 4.982

Review 5.  Pyruvate dehydrogenase deficiency.

Authors:  G K Brown; L J Otero; M LeGris; R M Brown
Journal:  J Med Genet       Date:  1994-11       Impact factor: 6.318

Review 6.  Metabolic disorders of embryogenesis.

Authors:  G K Brown
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

Review 7.  Pyruvate dehydrogenase E1 alpha deficiency.

Authors:  G K Brown
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

8.  Cortical metabolism in pyruvate dehydrogenase deficiency revealed by ex vivo multiplet (13)C NMR of the adult mouse brain.

Authors:  Isaac Marin-Valencia; Levi B Good; Qian Ma; Craig R Malloy; Mulchand S Patel; Juan M Pascual
Journal:  Neurochem Int       Date:  2012-08-03       Impact factor: 3.921

9.  Neuropathological findings of a patient with pyruvate dehydrogenase E1 alpha deficiency presenting as a cerebral lactic acidosis.

Authors:  A Michotte; L De Meirleir; W Lissens; R Denis; J L Wayenberg; I Liebaers; J M Brucher
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

10.  An amino acid substitution in the pyruvate dehydrogenase E1 alpha gene, affecting mitochondrial import of the precursor protein.

Authors:  F Takakubo; P Cartwright; N Hoogenraad; D R Thorburn; F Collins; T Lithgow; H H Dahl
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

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