Literature DB >> 4009207

The cerebro-hepato-renal (Zellweger) syndrome: lamellar lipid profiles in adrenocortical, hepatic mesenchymal, astrocyte cells and increased levels of very long chain fatty acids and phytanic acid in the plasma.

P Aubourg, O Robain, F Rocchiccioli, S Dancea, J Scotto.   

Abstract

Clinical, radiological, histological and biochemical aspects of two cases of cerebro-hepato-renal syndrome (CHRS) are reported. CT scan disclosed a demyelinating process and gyral abnormalities reflecting the observed neuropathological findings. Trilamellar and lamellar inclusions were found in brain astrocytes, hepatic mesenchymal and adrenal cells. The morphologic features of these inclusions are similar to those observed in childhood adrenoleukodystrophy, neonatal adrenoleukodystrophy and infantile Refsum's disease. In the two CHRS patients, increased plasma levels of very long chain fatty acids (C26:1, C26:0) and phytanic acid were in the same range as those observed in seven other instances of neonatal adrenoleukodystrophy. The presence of increased plasma levels of phytanic acid in these disorders suggests that phytanate oxidase activity is, at least, partially located in peroxisomes.

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Year:  1985        PMID: 4009207     DOI: 10.1016/0022-510x(85)90003-6

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  12 in total

1.  A pathological study of a peripheral nerve in a case of neonatal adrenoleukodystrophy.

Authors:  T Mito; K Takada; S Akaboshi; S Takashima; K Takeshita; Y Origuchi
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

2.  Neonatal adrenoleukodystrophy.

Authors:  P Aubourg; J Scotto; F Rocchiccioli; D Feldmann-Pautrat; O Robain
Journal:  J Neurol Neurosurg Psychiatry       Date:  1986-01       Impact factor: 10.154

3.  Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.

Authors:  B T Poll-The; J M Saudubray; H A Ogier; M Odièvre; J M Scotto; L Monnens; L C Govaerts; F Roels; A Cornelis; R B Schutgens
Journal:  Eur J Pediatr       Date:  1987-09       Impact factor: 3.183

4.  Immunocytochemical localization of serine: pyruvate aminotransferase in peroxisomes of the human liver parenchymal cells.

Authors:  S Yokota; T Oda; A Ichiyama
Journal:  Histochemistry       Date:  1987

Review 5.  Peroxisomal disorders: a newly recognised group of genetic diseases.

Authors:  R B Schutgens; H S Heymans; R J Wanders; H van den Bosch; J M Tager
Journal:  Eur J Pediatr       Date:  1986-02       Impact factor: 3.183

Review 6.  Organelle pathology in metabolic neuromuscular disease: an overview.

Authors:  L E Becker
Journal:  Can J Vet Res       Date:  1990-01       Impact factor: 1.310

7.  Pathology of hepatic peroxisomes and mitochondria in patients with peroxisomal disorders.

Authors:  J L Hughes; A Poulos; E Robertson; C W Chow; L J Sheffield; J Christodoulou; R F Carter
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1990

8.  Adrenoleukodystrophy: heterogeneity in two brothers.

Authors:  G M Elrington; D E Bateman; M J Jeffrey; N F Lawton
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-03       Impact factor: 10.154

9.  Unusual orthochromatic leukodystrophy with epitheloid cells (Norman-Gullotta): increase of very long chain fatty acids in brain discloses a peroxisomal disorder.

Authors:  B Molzer; F Gullotta; K Harzer; A Poulos; H Bernheimer
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

10.  Proton conductance caused by long-chain fatty acids in phospholipid bilayer membranes.

Authors:  J Gutknecht
Journal:  J Membr Biol       Date:  1988-11       Impact factor: 1.843

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