Literature DB >> 8213073

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

B Molzer1, F Gullotta, K Harzer, A Poulos, H Bernheimer.   

Abstract

Very long chain fatty acids (VLCFA) were found to be markedly increased and phytanic acid was borderline above normal in formalin-fixed brain white matter of case with an unusual type of familial leukodystrophy with epitheloid cells as described previously by Gullotta et al. [Neuropädiatrie (1970) 2: 173-186]. Increased VLCFA in brain clearly demonstrate that the patient had suffered from a peroxisomal disease. This diagnosis is corroborated by ultrastructural findings in brain showing typical lamellar inclusions. The particular type of peroxisomal disorder present in case (heterozygote of X-linked adrenoleukodystrophy?) remains speculative.

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Year:  1993        PMID: 8213073     DOI: 10.1007/bf00334888

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


  16 in total

1.  Adrenoleukodystrophy. A clinical and pathological study of 17 cases.

Authors:  H H Schaumburg; J M Powers; C S Raine; K Suzuki; E P Richardson
Journal:  Arch Neurol       Date:  1975-09

Review 2.  The inborn errors of peroxisomal beta-oxidation: a review.

Authors:  R J Wanders; C W van Roermund; R B Schutgens; P G Barth; H S Heymans; H van den Bosch; J M Tager
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  [Combination of Addison's and Schilder's disease in a woman aged 43 years (author's transl)].

Authors:  P Pilz; P Schiener
Journal:  Acta Neuropathol       Date:  1973-12-03       Impact factor: 17.088

4.  [Unusual orthochromatic leukodystrophy in three siblings].

Authors:  F Gullotta; R Heyer; G Tropitzsch; R Hormes; P Citoler
Journal:  Neuropadiatrie       Date:  1970-12

5.  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.

Authors:  P Aubourg; O Robain; F Rocchiccioli; S Dancea; J Scotto
Journal:  J Neurol Sci       Date:  1985 May-Jun       Impact factor: 3.181

6.  Neonatal-onset adrenoleukodystrophy in a girl.

Authors:  J E Haas; E S Johnson; D L Farrell
Journal:  Ann Neurol       Date:  1982-11       Impact factor: 10.422

7.  Accumulation of very long chain fatty acids is common to 3 variants of adrenoleukodystrophy (ALD). "Classical" ALD, atypical ALD (female patient) and adrenomyeloneuropathy.

Authors:  B Molzer; H Bernheimer; H Budka; P Pilz; K Toifl
Journal:  J Neurol Sci       Date:  1981-08       Impact factor: 3.181

8.  Addison disease and cerebral sclerosis in an apparently heterozygous girl: evidence for inactivation of the adrenoleukodystrophy locus.

Authors:  W Heffungs; H Hameister; H H Ropers
Journal:  Clin Genet       Date:  1980-09       Impact factor: 4.438

9.  Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder.

Authors:  Y Suzuki; N Shimozawa; T Orii; N Igarashi; N Kono; T Hashimoto
Journal:  Clin Chim Acta       Date:  1988-02-29       Impact factor: 3.786

10.  A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).

Authors:  B T Poll-The; F Roels; H Ogier; J Scotto; J Vamecq; R B Schutgens; R J Wanders; C W van Roermund; M J van Wijland; A W Schram
Journal:  Am J Hum Genet       Date:  1988-03       Impact factor: 11.025

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  1 in total

Review 1.  Neuropathology of peroxisomal diseases.

Authors:  J J Martin
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

  1 in total

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