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Peroxisomal disorders: A review

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Journal of Inherited Metabolic Disease

Summary

Until recently peroxisomal disorders were considered to be extremely rare and the diagnostic procedures available for postanatal and prenatal diagnosis were not widely known. At present, 17 human disorders are linked to peroxisomal dysfunction. The clinical, biochemical and morphological peroxisome heterogeneity described in the different diseases illustrate that only combined analysis of all the different approaches will lead to a correct diagnosis and a coherent pathophysiological model to guide ongoing research. With the study of human peroxisomal diseasese, advances have been gained as to the function of the peroxisome in normal and pathological conditions. Genetic analysis of peroxisome biogenesis and research on peroxisomal targeting signals are now in progress. Peroxisomal disorders are usually classified according to the degree of biochemical impairment. In this paper, a tentative classification of peroxisomal disorders will be proposed, based on the degree of biochemical abnormalities combined with new data obtained on whether or not defective peroxisome assembly is involved: (1) disorders with peroxisome assembly deficiencies; (2) disorders with single enzyme deficiencies.

The clinical onset and the major symptoms of the various disorders, and the recently discovered findings are discussed.

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Authors and Affiliations

  1. Department of Metabolic Diseases, University Children's Hospital, ‘Wilhelmina Kinderziekenhuis’, Nieuwe Gracht 137, 3512 LK, Utrecht, The Netherlands

    B. Fournier, J. A. M. Smeitink, L. Dorland, R. Berger & B. T. Poll-The

  2. Département de Pédiatrie, Hôpital des Enfants-Malades, 75743, Paris Cédex 15, France

    J. M. Saudubray

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  1. B. Fournier
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  2. J. A. M. Smeitink
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  3. L. Dorland
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  4. R. Berger
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  5. J. M. Saudubray
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  6. B. T. Poll-The
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Fournier, B., Smeitink, J.A.M., Dorland, L. et al. Peroxisomal disorders: A review. J Inherit Metab Dis 17, 470–486 (1994). https://doi.org/10.1007/BF00711362

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