Clinical approach to inherited peroxisomal disorders

@article{PoggiTravert2004ClinicalAT,
  title={Clinical approach to inherited peroxisomal disorders},
  author={F. Poggi-Travert and B. Fournier and B. Poll-The and J. Saudubray},
  journal={Journal of Inherited Metabolic Disease},
  year={2004},
  volume={18},
  pages={1-18}
}
SummaryAt least 21 genetic disorders have now been found that are linked to peroxisomal dysfunction. Whatever the genetic defect might be, peroxisomal disorders should be considered in various clinical conditions, dependent on the age of onset.The prototype of peroxisomal disorders is represented by ‘classical’ Zellweger syndrome (ZS) which is the most severe disorder combining all the characteristic symptoms. ZS is characterized by the association of errors of morphogenesis, severe… Expand
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